Canonical Allele Identifier: CA2551523716
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255383_133255387del , CM000671.2:g.133255383_133255387del GRCh38
NC_000009.11:g.136130770_136130774del , CM000671.1:g.136130770_136130774del GRCh37
NC_000009.10:g.135120591_135120595del NCBI36
NG_006669.1:g.22281_22285del
NG_006669.2:g.24829_24833del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1373_1377del
ENST00000647353.1:n.54-4235_54-4231del
ENST00000679909.1:c.28+19775_28+19779del ENSP00000506089.1:n.28+19775_28+19779del
ENST00000453660.3:n.1355_1359del
ENST00000611156.4:c.*279_*283del ENSP00000483265.1:n.*279_*283del
NM_020469.2:c.*279_*283del NP_065202.2:n.*279_*283del
NM_020469.3:c.*279_*283del NP_065202.2:n.*279_*283del