Canonical Allele Identifier: CA1882579839
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255914_133255915delinsAC , CM000671.2:g.133255914_133255915delinsAC GRCh38
NC_000009.11:g.136131301_136131302delinsAC , CM000671.1:g.136131301_136131302delinsAC GRCh37
NC_000009.10:g.135121122_135121123delinsAC NCBI36
NG_006669.1:g.21753_21754delinsGT
NG_006669.2:g.24301_24302delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.845_846delinsGT
ENST00000647353.1:n.54-4763_54-4762delinsGT
ENST00000679909.1:c.28+19247_28+19248delinsGT ENSP00000506089.1:n.28+19247_28+19248delinsGT
ENST00000453660.3:n.827_828delinsGT
ENST00000538324.2:c.813_814delinsGT ENSP00000483018.1:p.Gly271=
ENST00000611156.4:c.813_814delinsGT ENSP00000483265.1:p.Gly271=
NM_020469.2:c.816_817delinsGT NP_065202.2:p.Gly272=
NM_020469.3:c.816_817delinsGT NP_065202.2:p.Gly272=