Canonical Allele Identifier: CA1882579422
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255752G= , CM000671.2:g.133255752G= GRCh38
NC_000009.11:g.136131139G= , CM000671.1:g.136131139G= GRCh37
NC_000009.10:g.135120960G= NCBI36
NG_006669.1:g.21916C=
NG_006669.2:g.24464C=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.1008C=
ENST00000647353.1:n.54-4600C=
ENST00000679909.1:c.28+19410C= ENSP00000506089.1:n.28+19410C=
ENST00000453660.3:n.990C=
ENST00000538324.2:c.976C= ENSP00000483018.1:p.Gln326=
ENST00000611156.4:c.976C= ENSP00000483265.1:p.Gln326=
NM_020469.2:c.979C= NP_065202.2:p.Gln327=
NM_020469.3:c.979C= NP_065202.2:p.Gln327=