Canonical Allele Identifier: CA1882579115
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255628G= , CM000671.2:g.133255628G= GRCh38
NC_000009.11:g.136131015G= , CM000671.1:g.136131015G= GRCh37
NC_000009.10:g.135120836G= NCBI36
NG_006669.1:g.22040C=
NG_006669.2:g.24588C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1132C=
ENST00000647353.1:n.54-4476C=
ENST00000679909.1:c.28+19534C= ENSP00000506089.1:n.28+19534C=
ENST00000453660.3:n.1114C=
ENST00000538324.2:c.1096C= ENSP00000483018.1:p.Pro366=
ENST00000611156.4:c.*38C= ENSP00000483265.1:n.*38C=
NM_020469.2:c.*38C= NP_065202.2:n.*38C=
NM_020469.3:c.*38C= NP_065202.2:n.*38C=