Canonical Allele Identifier: CA2832563362
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255516dup , CM000671.2:g.133255516dup GRCh38
NC_000009.11:g.136130903dup , CM000671.1:g.136130903dup GRCh37
NC_000009.10:g.135120724dup NCBI36
NG_006669.1:g.22156dup
NG_006669.2:g.24704dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1248dup
ENST00000647353.1:n.54-4360dup
ENST00000679909.1:c.28+19650dup ENSP00000506089.1:n.28+19650dup
ENST00000453660.3:n.1230dup
ENST00000611156.4:c.*154dup ENSP00000483265.1:n.*154dup
NM_020469.2:c.*154dup NP_065202.2:n.*154dup
NM_020469.3:c.*154dup NP_065202.2:n.*154dup