Canonical Allele Identifier: CA982006217
Gene: TOP3A HGNC NCBI

Linked Data

dbSNP Id: rs10700487
gnomAD v3: 17-18271264-C-CGGGGGG
gnomAD v4: 17-18271264-C-CGGGGGG
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18271267_18271272dup , CM000679.2:g.18271267_18271272dup GRCh38
NC_000017.10:g.18174581_18174586dup , CM000679.1:g.18174581_18174586dup GRCh37
NC_000017.9:g.18115306_18115311dup NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011524001.2:c.*3532_*3537dup XP_011522303.1:n.*3532_*3537dup
XM_024450903.1:c.*3532_*3537dup XP_024306671.1:n.*3532_*3537dup
XR_001752601.2:n.6813_6818dup
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