Canonical Allele Identifier: CA200765562
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs909803724

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256266C>T , CM000671.2:g.133256266C>T GRCh38
NC_000009.11:g.136131653C>T , CM000671.1:g.136131653C>T GRCh37
NC_000009.10:g.135121474C>T NCBI36
NG_006669.1:g.21402G>A
NG_006669.2:g.23950G>A

Transcript Alleles

HGVS Amino-acid change
NM_020469.2:c.465G>A NP_065202.2:p.Gln155=
NM_020469.3:c.465G>A NP_065202.2:p.Gln155=
ENST00000453660.3:n.476G>A
ENST00000538324.2:c.462G>A ENSP00000483018.1:p.Gln154=
ENST00000611156.4:c.462G>A ENSP00000483265.1:p.Gln154=