Canonical Allele Identifier: CA1882582223
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257318C= , CM000671.2:g.133257318C= GRCh38
NC_000009.11:g.136132705C= , CM000671.1:g.136132705C= GRCh37
NC_000009.10:g.135122526C= NCBI36
NG_006669.1:g.20350G=
NG_006669.2:g.22898G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+91G=
ENST00000647353.1:n.54-6166G=
ENST00000651471.1:n.329+724G=
ENST00000679909.1:c.28+17844G= ENSP00000506089.1:n.28+17844G=
ENST00000453660.3:n.385+91G=
ENST00000538324.2:c.371+91G= ENSP00000483018.1:n.371+91G=
ENST00000611156.4:c.371+91G= ENSP00000483265.1:n.371+91G=
NM_020469.2:c.374+91G= NP_065202.2:n.374+91G=
NM_020469.3:c.374+91G= NP_065202.2:n.374+91G=