Canonical Allele Identifier: CA1882582317
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257458A= , CM000671.2:g.133257458A= GRCh38
NC_000009.11:g.136132845A= , CM000671.1:g.136132845A= GRCh37
NC_000009.10:g.135122666A= NCBI36
NG_006669.1:g.20210T=
NG_006669.2:g.22758T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.354T=
ENST00000647353.1:n.54-6306T=
ENST00000651471.1:n.329+584T=
ENST00000679909.1:c.28+17704T= ENSP00000506089.1:n.28+17704T=
ENST00000453660.3:n.336T=
ENST00000538324.2:c.322T= ENSP00000483018.1:p.Phe108=
ENST00000611156.4:c.322T= ENSP00000483265.1:p.Phe108=
NM_020469.2:c.325T= NP_065202.2:p.Phe109=
NM_020469.3:c.325T= NP_065202.2:p.Phe109=