Canonical Allele Identifier: CA1882580289
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256080G= , CM000671.2:g.133256080G= GRCh38
NC_000009.11:g.136131467G= , CM000671.1:g.136131467G= GRCh37
NC_000009.10:g.135121288G= NCBI36
NG_006669.1:g.21588C=
NG_006669.2:g.24136C=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.680C=
ENST00000647353.1:n.54-4928C=
ENST00000679909.1:c.28+19082C= ENSP00000506089.1:n.28+19082C=
ENST00000453660.3:n.662C=
ENST00000538324.2:c.648C= ENSP00000483018.1:p.Arg216=
ENST00000611156.4:c.648C= ENSP00000483265.1:p.Arg216=
NM_020469.2:c.651C= NP_065202.2:p.Arg217=
NM_020469.3:c.651C= NP_065202.2:p.Arg217=