Canonical Allele Identifier: CA1882582393
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257506G= , CM000671.2:g.133257506G= GRCh38
NC_000009.11:g.136132893G= , CM000671.1:g.136132893G= GRCh37
NC_000009.10:g.135122714G= NCBI36
NG_006669.1:g.20162C=
NG_006669.2:g.22710C=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.306C=
ENST00000647353.1:n.54-6354C=
ENST00000651471.1:n.329+536C=
ENST00000679909.1:c.28+17656C= ENSP00000506089.1:n.28+17656C=
ENST00000453660.3:n.288C=
ENST00000538324.2:c.274C= ENSP00000483018.1:p.Pro92=
ENST00000611156.4:c.274C= ENSP00000483265.1:p.Pro92=
NM_020469.2:c.277C= NP_065202.2:p.Pro93=
NM_020469.3:c.277C= NP_065202.2:p.Pro93=