Canonical Allele Identifier: CA1882582292
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257438_133257486delinsGGTGGTGTTCTGGAGCCTGAACTGCTCGTTGAGGATGTCGATGTTGAAT , CM000671.2:g.133257438_133257486delinsGGTGGTGTTCTGGAGCCTGAACTGCTCGTTGAGGATGTCGATGTTGAAT GRCh38
NC_000009.11:g.136132825_136132873delinsGGTGGTGTTCTGGAGCCTGAACTGCTCGTTGAGGATGTCGATGTTGAAT , CM000671.1:g.136132825_136132873delinsGGTGGTGTTCTGGAGCCTGAACTGCTCGTTGAGGATGTCGATGTTGAAT GRCh37
NC_000009.10:g.135122646_135122694delinsGGTGGTGTTCTGGAGCCTGAACTGCTCGTTGAGGATGTCGATGTTGAAT NCBI36
NG_006669.1:g.20182_20230delinsATTCAACATCGACATCCTCAACGAGCAGTTCAGGCTCCAGAACACCACC
NG_006669.2:g.22730_22778delinsATTCAACATCGACATCCTCAACGAGCAGTTCAGGCTCCAGAACACCACC

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.326_374delinsATTCAACATCGACATCCTCAACGAGCAGTTCAGGCTCCAGAACACCACC
ENST00000647353.1:n.54-6334_54-6286delinsATTCAACATCGACATCCTCAACGAGCAGTTCAGGCTCCAGAACACCACC
ENST00000651471.1:n.329+556_329+604delinsATTCAACATCGACATCCTCAACGAGCAGTTCAGGCTCCAGAACACCACC
ENST00000679909.1:c.28+17676_28+17724delinsATTCAACATCGACATCCTCAACGAGCAGTTCAGGCTCCAGAACACCACC ENSP00000506089.1:n.28+17676_28+17724deli...
ENST00000453660.3:n.308_356delinsATTCAACATCGACATCCTCAACGAGCAGTTCAGGCTCCAGAACACCACC
ENST00000538324.2:c.294_342delinsATTCAACATCGACATCCTCAACGAGCAGTTCAGGCTCCAGAACACCACC ENSP00000483018.1:p.Thr98=
ENST00000611156.4:c.294_342delinsATTCAACATCGACATCCTCAACGAGCAGTTCAGGCTCCAGAACACCACC ENSP00000483265.1:p.Thr98=
NM_020469.2:c.297_345delinsATTCAACATCGACATCCTCAACGAGCAGTTCAGGCTCCAGAACACCACC NP_065202.2:p.Thr99=
NM_020469.3:c.297_345delinsATTCAACATCGACATCCTCAACGAGCAGTTCAGGCTCCAGAACACCACC NP_065202.2:p.Thr99=