Canonical Allele Identifier: CA773571848

Gene: RAD51C

Linked Data

• dbSNP Id: rs1319598133
• gnomAD v3: 17-58692575-C-T
• gnomAD v4: 17-58692575-C-T
• MyVariant Identifiers: chr17:g.56769936C>T (hg19) ; chr17:g.58692575C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692575C>T , CM000679.2:g.58692575C>T	GRCh38
NC_000017.10:g.56769936C>T , CM000679.1:g.56769936C>T	GRCh37
NC_000017.9:g.54124935C>T	NCBI36
NG_023199.1:g.4974C>T , LRG_314:g.4974C>T
NG_047169.1:g.4505G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-317C>T	ENSP00000464056.2:n.-317C>T
ENST00000697675.1:n.3C>T
ENST00000337432.8:c.-69C>T	ENSP00000336701.4:n.-69C>T
ENST00000461271.5:c.-317C>T	ENSP00000464056.1:n.-317C>T
ENST00000583539.5:c.-69C>T	ENSP00000463121.1:n.-69C>T
NM_002876.3:c.-69C>T	NP_002867.1:n.-69C>T
NM_058216.2:c.-69C>T	NP_478123.1:n.-69C>T
NR_103872.1:n.3C>T
NR_103873.1:n.3C>T
XM_006722001.2:c.-69C>T	XP_006722064.1:n.-69C>T
XM_006722002.2:c.-69C>T	XP_006722065.1:n.-69C>T
XM_006722005.2:c.-264C>T	XP_006722068.1:n.-264C>T
XR_934513.1:n.5C>T
XR_934514.1:n.5C>T
XM_006722001.4:c.-69C>T	XP_006722064.1:n.-69C>T
XM_006722002.4:c.-69C>T	XP_006722065.1:n.-69C>T
XM_006722005.3:c.-264C>T	XP_006722068.1:n.-264C>T
XM_017024917.1:c.-264C>T	XP_016880406.1:n.-264C>T
XR_934513.3:n.436C>T
XR_934514.3:n.436C>T