Canonical Allele Identifier: CA2636471258
Gene: TOP3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18271378T>C , CM000679.2:g.18271378T>C GRCh38
NC_000017.10:g.18174692T>C , CM000679.1:g.18174692T>C GRCh37
NC_000017.9:g.18115417T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011524001.2:c.*3424A>G XP_011522303.1:n.*3424A>G
XM_024450903.1:c.*3424A>G XP_024306671.1:n.*3424A>G
XR_001752601.2:n.6705A>G