Canonical Allele Identifier: CA1882579828
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255912C= , CM000671.2:g.133255912C= GRCh38
NC_000009.11:g.136131299C= , CM000671.1:g.136131299C= GRCh37
NC_000009.10:g.135121120C= NCBI36
NG_006669.1:g.21756G=
NG_006669.2:g.24304G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.848G=
ENST00000647353.1:n.54-4760G=
ENST00000679909.1:c.28+19250G= ENSP00000506089.1:n.28+19250G=
ENST00000453660.3:n.830G=
ENST00000538324.2:c.816G= ENSP00000483018.1:p.Ser272=
ENST00000611156.4:c.816G= ENSP00000483265.1:p.Ser272=
NM_020469.2:c.819G= NP_065202.2:p.Ser273=
NM_020469.3:c.819G= NP_065202.2:p.Ser273=