Canonical Allele Identifier: CA292046569

Gene: RAD51C

Linked Data

• dbSNP Id: rs958870284
• gnomAD v2: 17-56769914-G-A
• gnomAD v3: 17-58692553-G-A
• gnomAD v4: 17-58692553-G-A
• MyVariant Identifiers: chr17:g.56769914G>A (hg19) ; chr17:g.58692553G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692553G>A , CM000679.2:g.58692553G>A	GRCh38
NC_000017.10:g.56769914G>A , CM000679.1:g.56769914G>A	GRCh37
NC_000017.9:g.54124913G>A	NCBI36
NG_023199.1:g.4952G>A , LRG_314:g.4952G>A
NG_047169.1:g.4527C>T

Transcript Alleles

HGVS	Amino-acid change
XM_006722005.2:c.-286G>A	XP_006722068.1:n.-286G>A
XM_006722001.4:c.-91G>A	XP_006722064.1:n.-91G>A
XM_006722002.4:c.-91G>A	XP_006722065.1:n.-91G>A
XM_006722005.3:c.-286G>A	XP_006722068.1:n.-286G>A
XM_017024917.1:c.-286G>A	XP_016880406.1:n.-286G>A
XR_934513.3:n.414G>A
XR_934514.3:n.414G>A