Canonical Allele Identifier: CA1882590531
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274075_133274076delinsTC , CM000671.2:g.133274075_133274076delinsTC GRCh38
NC_000009.11:g.136149491_136149492delinsTC , CM000671.1:g.136149491_136149492delinsTC GRCh37
NC_000009.10:g.135139312_135139313delinsTC NCBI36
NG_006669.1:g.3559_3560delinsGA
NG_006669.2:g.6139_6140delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.58+1086_58+1087delinsGA
ENST00000647353.1:n.53+1086_53+1087delinsGA
ENST00000651471.1:n.63+1886_63+1887delinsGA
ENST00000679909.1:c.28+1086_28+1087delinsGA ENSP00000506089.1:n.28+1086_28+1087delinsGA
ENST00000453660.3:n.40+1086_40+1087delinsGA
ENST00000538324.2:c.28+1086_28+1087delinsGA ENSP00000483018.1:n.28+1086_28+1087delinsGA
ENST00000611156.4:c.28+1086_28+1087delinsGA ENSP00000483265.1:n.28+1086_28+1087delinsGA
NM_020469.2:c.28+1086_28+1087delinsGA NP_065202.2:n.28+1086_28+1087delinsGA
NM_020469.3:c.28+1086_28+1087delinsGA NP_065202.2:n.28+1086_28+1087delinsGA