Canonical Allele Identifier: CA2839095968
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257458dup , CM000671.2:g.133257458dup GRCh38
NC_000009.11:g.136132845dup , CM000671.1:g.136132845dup GRCh37
NC_000009.10:g.135122666dup NCBI36
NG_006669.1:g.20211dup
NG_006669.2:g.22759dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.355dup
ENST00000647353.1:n.54-6305dup
ENST00000651471.1:n.329+585dup
ENST00000679909.1:c.28+17705dup ENSP00000506089.1:n.28+17705dup
ENST00000453660.3:n.337dup
ENST00000538324.2:c.323dup ENSP00000483018.1:p.Arg109GlnfsTer?
ENST00000611156.4:c.323dup ENSP00000483265.1:p.Arg109GlnfsTer?
NM_020469.2:c.326dup NP_065202.2:p.Arg110GlnfsTer?
NM_020469.3:c.326dup NP_065202.2:p.Arg110GlnfsTer?