Canonical Allele Identifier: CA375686697
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257490C>T , CM000671.2:g.133257490C>T GRCh38
NC_000009.11:g.136132877C>T , CM000671.1:g.136132877C>T GRCh37
NC_000009.10:g.135122698C>T NCBI36
NG_006669.1:g.20178G>A
NG_006669.2:g.22726G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.322G>A
ENST00000647353.1:n.54-6338G>A
ENST00000651471.1:n.329+552G>A
ENST00000679909.1:c.28+17672G>A ENSP00000506089.1:n.28+17672G>A
ENST00000453660.3:n.304G>A
ENST00000538324.2:c.290G>A ENSP00000483018.1:p.Gly97Asp
ENST00000611156.4:c.290G>A ENSP00000483265.1:p.Gly97Asp
NM_020469.2:c.293G>A NP_065202.2:p.Gly98Asp
NM_020469.3:c.293G>A NP_065202.2:p.Gly98Asp