Canonical Allele Identifier: CA1882580080
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255992C= , CM000671.2:g.133255992C= GRCh38
NC_000009.11:g.136131379C= , CM000671.1:g.136131379C= GRCh37
NC_000009.10:g.135121200C= NCBI36
NG_006669.1:g.21676G=
NG_006669.2:g.24224G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.768G=
ENST00000647353.1:n.54-4840G=
ENST00000679909.1:c.28+19170G= ENSP00000506089.1:n.28+19170G=
ENST00000453660.3:n.750G=
ENST00000538324.2:c.736G= ENSP00000483018.1:p.Glu246=
ENST00000611156.4:c.736G= ENSP00000483265.1:p.Glu246=
NM_020469.2:c.739G= NP_065202.2:p.Glu247=
NM_020469.3:c.739G= NP_065202.2:p.Glu247=