Canonical Allele Identifier: CA1882579642
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255836_133255849delinsCGGCCTCGATGCCG , CM000671.2:g.133255836_133255849delinsCGGCCTCGATGCCG GRCh38
NC_000009.11:g.136131223_136131236delinsCGGCCTCGATGCCG , CM000671.1:g.136131223_136131236delinsCGGCCTCGATGCCG GRCh37
NC_000009.10:g.135121044_135121057delinsCGGCCTCGATGCCG NCBI36
NG_006669.1:g.21819_21832delinsCGGCATCGAGGCCG
NG_006669.2:g.24367_24380delinsCGGCATCGAGGCCG

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.911_924delinsCGGCATCGAGGCCG
ENST00000647353.1:n.54-4697_54-4684delinsCGGCATCGAGGCCG
ENST00000679909.1:c.28+19313_28+19326delinsCGGCATCGAGGCCG ENSP00000506089.1:n.28+19313_28+19326deli...
ENST00000453660.3:n.893_906delinsCGGCATCGAGGCCG
ENST00000538324.2:c.879_892delinsCGGCATCGAGGCCG ENSP00000483018.1:p.Asn293=
ENST00000611156.4:c.879_892delinsCGGCATCGAGGCCG ENSP00000483265.1:p.Asn293=
NM_020469.2:c.882_895delinsCGGCATCGAGGCCG NP_065202.2:p.Asn294=
NM_020469.3:c.882_895delinsCGGCATCGAGGCCG NP_065202.2:p.Asn294=