Canonical Allele Identifier: CA375686311
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256270T>A , CM000671.2:g.133256270T>A GRCh38
NC_000009.11:g.136131657T>A , CM000671.1:g.136131657T>A GRCh37
NC_000009.10:g.135121478T>A NCBI36
NG_006669.1:g.21398A>T
NG_006669.2:g.23946A>T

Transcript Alleles

HGVS Amino-acid change
NM_020469.2:c.461A>T NP_065202.2:p.Asp154Val
NM_020469.3:c.461A>T NP_065202.2:p.Asp154Val
ENST00000453660.3:n.472A>T
ENST00000538324.2:c.458A>T ENSP00000483018.1:p.Asp153Val
ENST00000611156.4:c.458A>T ENSP00000483265.1:p.Asp153Val