Canonical Allele Identifier: CA1882580175
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256025_133256030delinsAGCCGG , CM000671.2:g.133256025_133256030delinsAGCCGG GRCh38
NC_000009.11:g.136131412_136131417delinsAGCCGG , CM000671.1:g.136131412_136131417delinsAGCCGG GRCh37
NC_000009.10:g.135121233_135121238delinsAGCCGG NCBI36
NG_006669.1:g.21638_21643delinsCCGGCT
NG_006669.2:g.24186_24191delinsCCGGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.730_735delinsCCGGCT
ENST00000647353.1:n.54-4878_54-4873delinsCCGGCT
ENST00000679909.1:c.28+19132_28+19137delinsCCGGCT ENSP00000506089.1:n.28+19132_28+19137delinsCCGGCT
ENST00000453660.3:n.712_717delinsCCGGCT
ENST00000538324.2:c.698_703delinsCCGGCT ENSP00000483018.1:p.Pro233=
ENST00000611156.4:c.698_703delinsCCGGCT ENSP00000483265.1:p.Pro233=
NM_020469.2:c.701_706delinsCCGGCT NP_065202.2:p.Pro234=
NM_020469.3:c.701_706delinsCCGGCT NP_065202.2:p.Pro234=