Canonical Allele Identifier: CA1882579664
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255843G= , CM000671.2:g.133255843G= GRCh38
NC_000009.11:g.136131230G= , CM000671.1:g.136131230G= GRCh37
NC_000009.10:g.135121051G= NCBI36
NG_006669.1:g.21825C=
NG_006669.2:g.24373C=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.917C=
ENST00000647353.1:n.54-4691C=
ENST00000679909.1:c.28+19319C= ENSP00000506089.1:n.28+19319C=
ENST00000453660.3:n.899C=
ENST00000538324.2:c.885C= ENSP00000483018.1:p.Ile295=
ENST00000611156.4:c.885C= ENSP00000483265.1:p.Ile295=
NM_020469.2:c.888C= NP_065202.2:p.Ile296=
NM_020469.3:c.888C= NP_065202.2:p.Ile296=