Canonical Allele Identifier: CA1882580821
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256266C= , CM000671.2:g.133256266C= GRCh38
NC_000009.11:g.136131653C= , CM000671.1:g.136131653C= GRCh37
NC_000009.10:g.135121474C= NCBI36
NG_006669.1:g.21402G=
NG_006669.2:g.23950G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.494G=
ENST00000647353.1:n.54-5114G=
ENST00000651471.1:n.420G=
ENST00000679909.1:c.28+18896G= ENSP00000506089.1:n.28+18896G=
ENST00000453660.3:n.476G=
ENST00000538324.2:c.462G= ENSP00000483018.1:p.Gln154=
ENST00000611156.4:c.462G= ENSP00000483265.1:p.Gln154=
NM_020469.2:c.465G= NP_065202.2:p.Gln155=
NM_020469.3:c.465G= NP_065202.2:p.Gln155=