Canonical Allele Identifier: CA1882582217
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257314C= , CM000671.2:g.133257314C= GRCh38
NC_000009.11:g.136132701C= , CM000671.1:g.136132701C= GRCh37
NC_000009.10:g.135122522C= NCBI36
NG_006669.1:g.20354G=
NG_006669.2:g.22902G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+95G=
ENST00000647353.1:n.54-6162G=
ENST00000651471.1:n.329+728G=
ENST00000679909.1:c.28+17848G= ENSP00000506089.1:n.28+17848G=
ENST00000453660.3:n.385+95G=
ENST00000538324.2:c.371+95G= ENSP00000483018.1:n.371+95G=
ENST00000611156.4:c.371+95G= ENSP00000483265.1:n.371+95G=
NM_020469.2:c.374+95G= NP_065202.2:n.374+95G=
NM_020469.3:c.374+95G= NP_065202.2:n.374+95G=