Canonical Allele Identifier: CA375686332
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256280C>A , CM000671.2:g.133256280C>A GRCh38
NC_000009.11:g.136131667C>A , CM000671.1:g.136131667C>A GRCh37
NC_000009.10:g.135121488C>A NCBI36
NG_006669.1:g.21388G>T
NG_006669.2:g.23936G>T

Transcript Alleles

HGVS Amino-acid change
NM_020469.2:c.451G>T NP_065202.2:p.Val151Phe
NM_020469.3:c.451G>T NP_065202.2:p.Val151Phe
ENST00000453660.3:n.462G>T
ENST00000538324.2:c.448G>T ENSP00000483018.1:p.Val150Phe
ENST00000611156.4:c.448G>T ENSP00000483265.1:p.Val150Phe