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Identification of a novel B allele with a nucleotide deletion (c.103_106 delG) in the ABO gene associated with a B weak phenotype.

Transfusion - 1 Mar 2021

He Yunlei, Yu Lu, Xu Deyi, Zhang Jiwei, Deng Gang

Abstract excerpt

No abstract is available from the source.

Topics

ABO Blood-Group System
Alleles
Asian People
Exons
Genotype
Haplotypes
Humans
Male
Phenotype
Sequence Deletion

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 33615482
DOI: 10.1111/trf.16302

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

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Identification of a novel B allele with a nucleotide deletion (c.103_106 delG) in the ABO gene associated with a B weak phenotype.PMID 33615482Read ↗

ABO*B.01+c.464A>C represents a missense variation in the ABO gene and encodes a weak B phenotype.Semantic proximity Read ↗

Identification of a novel B allele with missense mutation (c.98G > C) in the ABO gene.Semantic proximity Read ↗

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Identification of a novel B allele with a c.256G>A mutation on the ABO*B.01 allele.Semantic proximity Read ↗

Identification of a novel B allele with a c.917 T > C mutation on the ABO*B.01 allele.Semantic proximity Read ↗

A novel B variant allele with c.586T>C (p.Cys196Arg) mutation identified at the ABO locus.Semantic proximity Read ↗

Identification of a novel A allele with a nucleotide deletion c.198delG in the ABO gene associated with Ael phenotype.Semantic proximity Read ↗

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Identification of a novel A allele with initiator codon variant (c.2T > A) in the ABO gene associated with weak A phenotype.Semantic proximity Read ↗

Identification of a novel A allele with a nucleotide insert (c.99-1_100 T) in the ABO gene associated with a A3 phenotype individual.Semantic proximity Read ↗

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Identification of a novel A allele with a c.36-39delA on the ABO*A1.02 allele.Semantic proximity Read ↗

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