Canonical Allele Identifier: CA1882590562
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274140_133274142delinsCAG , CM000671.2:g.133274140_133274142delinsCAG GRCh38
NC_000009.11:g.136149556_136149558delinsCAG , CM000671.1:g.136149556_136149558delinsCAG GRCh37
NC_000009.10:g.135139377_135139379delinsCAG NCBI36
NG_006669.1:g.3493_3495delinsCTG
NG_006669.2:g.6073_6075delinsCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.58+1020_58+1022delinsCTG
ENST00000647353.1:n.53+1020_53+1022delinsCTG
ENST00000651471.1:n.63+1820_63+1822delinsCTG
ENST00000679909.1:c.28+1020_28+1022delinsCTG ENSP00000506089.1:n.28+1020_28+1022delins...
ENST00000453660.3:n.40+1020_40+1022delinsCTG
ENST00000538324.2:c.28+1020_28+1022delinsCTG ENSP00000483018.1:n.28+1020_28+1022delins...
ENST00000611156.4:c.28+1020_28+1022delinsCTG ENSP00000483265.1:n.28+1020_28+1022delins...
NM_020469.2:c.28+1020_28+1022delinsCTG NP_065202.2:n.28+1020_28+1022delinsCTG
NM_020469.3:c.28+1020_28+1022delinsCTG NP_065202.2:n.28+1020_28+1022delinsCTG