Canonical Allele Identifier: CA2636471273
Gene: TOP3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18271389T>C , CM000679.2:g.18271389T>C GRCh38
NC_000017.10:g.18174703T>C , CM000679.1:g.18174703T>C GRCh37
NC_000017.9:g.18115428T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011524001.2:c.*3413A>G XP_011522303.1:n.*3413A>G
XM_024450903.1:c.*3413A>G XP_024306671.1:n.*3413A>G
XR_001752601.2:n.6694A>G