Canonical Allele Identifier: CA982006238
Gene: TOP3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18271272_18271273insGGGGGGGGG , CM000679.2:g.18271272_18271273insGGGGGGGGG GRCh38
NC_000017.10:g.18174586_18174587insGGGGGGGGG , CM000679.1:g.18174586_18174587insGGGGGGGGG GRCh37
NC_000017.9:g.18115311_18115312insGGGGGGGGG NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011524001.2:c.*3537_*3538insCCCCCCCCC XP_011522303.1:n.*3537_*3538insCCCCCCCCC
XM_024450903.1:c.*3537_*3538insCCCCCCCCC XP_024306671.1:n.*3537_*3538insCCCCCCCCC
XR_001752601.2:n.6818_6819insCCCCCCCCC