Canonical Allele Identifier: CA1882580254
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256050_133256085delinsCGGAGTCAGGATCTCCACGCCCACGTGGTCGCGGAA , CM000671.2:g.133256050_133256085delinsCGGAGTCAGGATCTCCACGCCCACGTGGTCGCGGAA GRCh38
NC_000009.11:g.136131437_136131472delinsCGGAGTCAGGATCTCCACGCCCACGTGGTCGCGGAA , CM000671.1:g.136131437_136131472delinsCGGAGTCAGGATCTCCACGCCCACGTGGTCGCGGAA GRCh37
NC_000009.10:g.135121258_135121293delinsCGGAGTCAGGATCTCCACGCCCACGTGGTCGCGGAA NCBI36
NG_006669.1:g.21583_21618delinsTTCCGCGACCACGTGGGCGTGGAGATCCTGACTCCG
NG_006669.2:g.24131_24166delinsTTCCGCGACCACGTGGGCGTGGAGATCCTGACTCCG

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.675_710delinsTTCCGCGACCACGTGGGCGTGGAGATCCTGACTCCG
ENST00000647353.1:n.54-4933_54-4898delinsTTCCGCGACCACGTGGGCGTGGAGATCCTGACTCCG
ENST00000679909.1:c.28+19077_28+19112delinsTTCCGCGACCACGTGGGCGTGGAGATCCTGACTCCG ENSP00000506089.1:n.28+19077_28+19112deli...
ENST00000453660.3:n.657_692delinsTTCCGCGACCACGTGGGCGTGGAGATCCTGACTCCG
ENST00000538324.2:c.643_678delinsTTCCGCGACCACGTGGGCGTGGAGATCCTGACTCCG ENSP00000483018.1:p.Phe215=
ENST00000611156.4:c.643_678delinsTTCCGCGACCACGTGGGCGTGGAGATCCTGACTCCG ENSP00000483265.1:p.Phe215=
NM_020469.2:c.646_681delinsTTCCGCGACCACGTGGGCGTGGAGATCCTGACTCCG NP_065202.2:p.Phe216=
NM_020469.3:c.646_681delinsTTCCGCGACCACGTGGGCGTGGAGATCCTGACTCCG NP_065202.2:p.Phe216=