Canonical Allele Identifier: CA292046521

Gene: RAD51C

Linked Data

• dbSNP Id: rs1009246645
• gnomAD v3: 17-58692543-C-G
• gnomAD v4: 17-58692543-C-G
• MyVariant Identifiers: chr17:g.56769904C>G (hg19) ; chr17:g.58692543C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692543C>G , CM000679.2:g.58692543C>G	GRCh38
NC_000017.10:g.56769904C>G , CM000679.1:g.56769904C>G	GRCh37
NC_000017.9:g.54124903C>G	NCBI36
NG_023199.1:g.4942C>G , LRG_314:g.4942C>G
NG_047169.1:g.4537G>C

Transcript Alleles

HGVS	Amino-acid change
XM_006722005.2:c.-296C>G	XP_006722068.1:n.-296C>G
XM_006722001.4:c.-101C>G	XP_006722064.1:n.-101C>G
XM_006722002.4:c.-101C>G	XP_006722065.1:n.-101C>G
XM_006722005.3:c.-296C>G	XP_006722068.1:n.-296C>G
XM_017024917.1:c.-296C>G	XP_016880406.1:n.-296C>G
XR_934513.3:n.404C>G
XR_934514.3:n.404C>G