Canonical Allele Identifier: CA467852784
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1382334176

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255978C>T , CM000671.2:g.133255978C>T GRCh38
NC_000009.11:g.136131365C>T , CM000671.1:g.136131365C>T GRCh37
NC_000009.10:g.135121186C>T NCBI36
NG_006669.1:g.21690G>A
NG_006669.2:g.24238G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.782G>A
ENST00000647353.1:n.54-4826G>A
ENST00000679909.1:c.28+19184G>A ENSP00000506089.1:n.28+19184G>A
ENST00000453660.3:n.764G>A
ENST00000538324.2:c.750G>A ENSP00000483018.1:p.Gln250=
ENST00000611156.4:c.750G>A ENSP00000483265.1:p.Gln250=
NM_020469.2:c.753G>A NP_065202.2:p.Gln251=
NM_020469.3:c.753G>A NP_065202.2:p.Gln251=