Canonical Allele Identifier: CA1882580495
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256155G= , CM000671.2:g.133256155G= GRCh38
NC_000009.11:g.136131542G= , CM000671.1:g.136131542G= GRCh37
NC_000009.10:g.135121363G= NCBI36
NG_006669.1:g.21513C=
NG_006669.2:g.24061C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.605C=
ENST00000647353.1:n.54-5003C=
ENST00000651471.1:n.531C=
ENST00000679909.1:c.28+19007C= ENSP00000506089.1:n.28+19007C=
ENST00000453660.3:n.587C=
ENST00000538324.2:c.573C= ENSP00000483018.1:p.Ile191=
ENST00000611156.4:c.573C= ENSP00000483265.1:p.Ile191=
NM_020469.2:c.576C= NP_065202.2:p.Ile192=
NM_020469.3:c.576C= NP_065202.2:p.Ile192=