Canonical Allele Identifier: CA375686320
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256274T>G , CM000671.2:g.133256274T>G GRCh38
NC_000009.11:g.136131661T>G , CM000671.1:g.136131661T>G GRCh37
NC_000009.10:g.135121482T>G NCBI36
NG_006669.1:g.21394A>C
NG_006669.2:g.23942A>C

Transcript Alleles

HGVS Amino-acid change
NM_020469.2:c.457A>C NP_065202.2:p.Thr153Pro
NM_020469.3:c.457A>C NP_065202.2:p.Thr153Pro
ENST00000453660.3:n.468A>C
ENST00000538324.2:c.454A>C ENSP00000483018.1:p.Thr152Pro
ENST00000611156.4:c.454A>C ENSP00000483265.1:p.Thr152Pro