Canonical Allele Identifier: CA375686310
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256269G>T , CM000671.2:g.133256269G>T GRCh38
NC_000009.11:g.136131656G>T , CM000671.1:g.136131656G>T GRCh37
NC_000009.10:g.135121477G>T NCBI36
NG_006669.1:g.21399C>A
NG_006669.2:g.23947C>A

Transcript Alleles

HGVS Amino-acid change
NM_020469.2:c.462C>A NP_065202.2:p.Asp154Glu
NM_020469.3:c.462C>A NP_065202.2:p.Asp154Glu
ENST00000453660.3:n.473C>A
ENST00000538324.2:c.459C>A ENSP00000483018.1:p.Asp153Glu
ENST00000611156.4:c.459C>A ENSP00000483265.1:p.Asp153Glu