Canonical Allele Identifier: CA1882583238
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258192_133258193delinsAG , CM000671.2:g.133258192_133258193delinsAG GRCh38
NG_006669.2:g.22022_22023delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.234-61_234-60delinsCT
ENST00000647353.1:n.54-7041_54-7040delinsCT
ENST00000651471.1:n.239-61_239-60delinsCT
ENST00000679909.1:c.28+16969_28+16970delinsCT ENSP00000506089.1:n.28+16969_28+16970delinsCT
ENST00000453660.3:n.216-61_216-60delinsCT
ENST00000538324.2:c.204-61_204-60delinsCT ENSP00000483018.1:n.204-61_204-60delinsCT
ENST00000611156.4:c.204-61_204-60delinsCT ENSP00000483265.1:n.204-61_204-60delinsCT
NM_020469.2:c.204-61_204-60delinsCT NP_065202.2:n.204-61_204-60delinsCT
NM_020469.3:c.204-61_204-60delinsCT NP_065202.2:n.204-61_204-60delinsCT