Canonical Allele Identifier: CA292046446
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs572500997

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692519G>A , CM000679.2:g.58692519G>A GRCh38
NC_000017.10:g.56769880G>A , CM000679.1:g.56769880G>A GRCh37
NC_000017.9:g.54124879G>A NCBI36
NG_023199.1:g.4918G>A , LRG_314:g.4918G>A
NG_047169.1:g.4561C>T

Transcript Alleles

HGVS Amino-acid change
XM_006722001.4:c.-125G>A XP_006722064.1:n.-125G>A
XM_006722002.4:c.-125G>A XP_006722065.1:n.-125G>A
XR_934513.3:n.380G>A
XR_934514.3:n.380G>A