Canonical Allele Identifier: CA1882579228
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs56392308
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255671_133255672del , CM000671.2:g.133255671_133255672del GRCh38
NC_000009.11:g.136131058_136131059del , CM000671.1:g.136131058_136131059del GRCh37
NC_000009.10:g.135120879_135120880del NCBI36
NG_006669.1:g.21997_21998del
NG_006669.2:g.24545_24546del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1089_1090del
ENST00000647353.1:n.54-4519_54-4518del
ENST00000679909.1:c.28+19491_28+19492del ENSP00000506089.1:n.28+19491_28+19492del
ENST00000453660.3:n.1071_1072del
ENST00000538324.2:c.1054-1_1054del
ENST00000611156.4:c.1057_1058del ENSP00000483265.1:p.Pro353ValfsTer?
NM_020469.2:c.1060_1061del NP_065202.2:p.Pro354ValfsTer?
NM_020469.3:c.1060_1061del NP_065202.2:p.Pro354ValfsTer?
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