Canonical Allele Identifier: CA1882582308
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257453C= , CM000671.2:g.133257453C= GRCh38
NC_000009.11:g.136132840C= , CM000671.1:g.136132840C= GRCh37
NC_000009.10:g.135122661C= NCBI36
NG_006669.1:g.20215G=
NG_006669.2:g.22763G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.359G=
ENST00000647353.1:n.54-6301G=
ENST00000651471.1:n.329+589G=
ENST00000679909.1:c.28+17709G= ENSP00000506089.1:n.28+17709G=
ENST00000453660.3:n.341G=
ENST00000538324.2:c.327G= ENSP00000483018.1:p.Arg109=
ENST00000611156.4:c.327G= ENSP00000483265.1:p.Arg109=
NM_020469.2:c.330G= NP_065202.2:p.Arg110=
NM_020469.3:c.330G= NP_065202.2:p.Arg110=