Canonical Allele Identifier: CA2638988572

Gene: RAD51C

Linked Data

• dbSNP Id: rs2143666059
• gnomAD v4: 17-58692558-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692558T>C , CM000679.2:g.58692558T>C	GRCh38
NC_000017.10:g.56769919T>C , CM000679.1:g.56769919T>C	GRCh37
NC_000017.9:g.54124918T>C	NCBI36
NG_023199.1:g.4957T>C , LRG_314:g.4957T>C
NG_047169.1:g.4522A>G

Transcript Alleles

HGVS	Amino-acid change
XM_006722005.2:c.-281T>C	XP_006722068.1:n.-281T>C
XM_006722001.4:c.-86T>C	XP_006722064.1:n.-86T>C
XM_006722002.4:c.-86T>C	XP_006722065.1:n.-86T>C
XM_006722005.3:c.-281T>C	XP_006722068.1:n.-281T>C
XM_017024917.1:c.-281T>C	XP_016880406.1:n.-281T>C
XR_934513.3:n.419T>C
XR_934514.3:n.419T>C