Canonical Allele Identifier: CA5305697
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs781867861

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255849G>A , CM000671.2:g.133255849G>A GRCh38
NC_000009.11:g.136131236G>A , CM000671.1:g.136131236G>A GRCh37
NC_000009.10:g.135121057G>A NCBI36
NG_006669.1:g.21819C>T
NG_006669.2:g.24367C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.911C>T
ENST00000647353.1:n.54-4697C>T
ENST00000679909.1:c.28+19313C>T ENSP00000506089.1:n.28+19313C>T
ENST00000453660.3:n.893C>T
ENST00000538324.2:c.879C>T ENSP00000483018.1:p.Asn293=
ENST00000611156.4:c.879C>T ENSP00000483265.1:p.Asn293=
NM_020469.2:c.882C>T NP_065202.2:p.Asn294=
NM_020469.3:c.882C>T NP_065202.2:p.Asn294=