Canonical Allele Identifier: CA375686319
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
NM_020469.2:c.457A>T NP_065202.2:p.Thr153Ser
NM_020469.3:c.457A>T NP_065202.2:p.Thr153Ser
ENST00000453660.3:n.468A>T
ENST00000538324.2:c.454A>T ENSP00000483018.1:p.Thr152Ser
ENST00000611156.4:c.454A>T ENSP00000483265.1:p.Thr152Ser