Canonical Allele Identifier: CA625045294
Gene: TOP3A HGNC NCBI

Linked Data

dbSNP Id: rs10700487
gnomAD v2: 17-18174578-C-CGGGGGGGGGGGGGGG
gnomAD v3: 17-18271264-C-CGGGGGGGGGGGGGGG
gnomAD v4: 17-18271264-C-CGGGGGGGGGGGGGGG
MyVariant Identifiers: chr17:g.18174578_18174579insGGGGGGGGGGGGGGG (hg19) chr17:g.18271264_18271265insGGGGGGGGGGGGGGG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18271272_18271273insGGGGGGGGGGGGGGG , CM000679.2:g.18271272_18271273insGGGGGGGGGGGGGGG GRCh38
NC_000017.10:g.18174586_18174587insGGGGGGGGGGGGGGG , CM000679.1:g.18174586_18174587insGGGGGGGGGGGGGGG GRCh37
NC_000017.9:g.18115311_18115312insGGGGGGGGGGGGGGG NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011524001.2:c.*3537_*3538insCCCCCCCCCCCCCCC XP_011522303.1:n.*3537_*3538insCCCCCCCCCC...
XM_024450903.1:c.*3537_*3538insCCCCCCCCCCCCCCC XP_024306671.1:n.*3537_*3538insCCCCCCCCCC...
XR_001752601.2:n.6818_6819insCCCCCCCCCCCCCCC
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