Canonical Allele Identifier: CA1882579085
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255618G= , CM000671.2:g.133255618G= GRCh38
NC_000009.11:g.136131005G= , CM000671.1:g.136131005G= GRCh37
NC_000009.10:g.135120826G= NCBI36
NG_006669.1:g.22050C=
NG_006669.2:g.24598C=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.1142C=
ENST00000647353.1:n.54-4466C=
ENST00000679909.1:c.28+19544C= ENSP00000506089.1:n.28+19544C=
ENST00000453660.3:n.1124C=
ENST00000538324.2:c.1106C= ENSP00000483018.1:p.Ser369=
ENST00000611156.4:c.*48C= ENSP00000483265.1:n.*48C=
NM_020469.2:c.*48C= NP_065202.2:n.*48C=
NM_020469.3:c.*48C= NP_065202.2:n.*48C=