Canonical Allele Identifier: CA1882590555
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274126_133274130delinsAGCAT , CM000671.2:g.133274126_133274130delinsAGCAT GRCh38
NC_000009.11:g.136149542_136149546delinsAGCAT , CM000671.1:g.136149542_136149546delinsAGCAT GRCh37
NC_000009.10:g.135139363_135139367delinsAGCAT NCBI36
NG_006669.1:g.3505_3509delinsATGCT
NG_006669.2:g.6085_6089delinsATGCT

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.58+1032_58+1036delinsATGCT
ENST00000647353.1:n.53+1032_53+1036delinsATGCT
ENST00000651471.1:n.63+1832_63+1836delinsATGCT
ENST00000679909.1:c.28+1032_28+1036delinsATGCT ENSP00000506089.1:n.28+1032_28+1036delins...
ENST00000453660.3:n.40+1032_40+1036delinsATGCT
ENST00000538324.2:c.28+1032_28+1036delinsATGCT ENSP00000483018.1:n.28+1032_28+1036delins...
ENST00000611156.4:c.28+1032_28+1036delinsATGCT ENSP00000483265.1:n.28+1032_28+1036delins...
NM_020469.2:c.28+1032_28+1036delinsATGCT NP_065202.2:n.28+1032_28+1036delinsATGCT
NM_020469.3:c.28+1032_28+1036delinsATGCT NP_065202.2:n.28+1032_28+1036delinsATGCT