Canonical Allele Identifier: CA1882582423
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257519G= , CM000671.2:g.133257519G= GRCh38
NC_000009.11:g.136132906G= , CM000671.1:g.136132906G= GRCh37
NC_000009.10:g.135122727G= NCBI36
NG_006669.1:g.20149C=
NG_006669.2:g.22697C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.293C=
ENST00000647353.1:n.54-6367C=
ENST00000651471.1:n.329+523C=
ENST00000679909.1:c.28+17643C= ENSP00000506089.1:n.28+17643C=
ENST00000453660.3:n.275C=
ENST00000538324.2:c.261C= ENSP00000483018.1:p.Thr87=
ENST00000611156.4:c.261C= ENSP00000483265.1:p.Thr87=
NM_020469.2:c.264C= NP_065202.2:p.Thr88=
NM_020469.3:c.264C= NP_065202.2:p.Thr88=