Canonical Allele Identifier: CA8677089

Gene: RAD51C

Linked Data

• dbSNP Id: rs765425309
• ExAC: 17:56769956 C / T
• gnomAD v2: 17-56769956-C-T
• gnomAD v4: 17-58692595-C-T
• MyVariant Identifiers: chr17:g.56769956C>T (hg19) ; chr17:g.58692595C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692595C>T , CM000679.2:g.58692595C>T	GRCh38
NC_000017.10:g.56769956C>T , CM000679.1:g.56769956C>T	GRCh37
NC_000017.9:g.54124955C>T	NCBI36
NG_023199.1:g.4994C>T , LRG_314:g.4994C>T
NG_047169.1:g.4485G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-297C>T	ENSP00000464056.2:n.-297C>T
ENST00000697675.1:n.23C>T
ENST00000697676.1:n.12C>T
ENST00000697677.1:n.10C>T
ENST00000697678.1:n.10C>T
ENST00000697679.1:n.3C>T
ENST00000697680.1:c.-49C>T	ENSP00000513392.1:n.-49C>T
ENST00000697681.1:c.-49C>T	ENSP00000513393.1:n.-49C>T
ENST00000697683.1:c.-49C>T	ENSP00000513395.1:n.-49C>T
ENST00000697684.1:n.12C>T
ENST00000697685.1:c.-49C>T	ENSP00000513396.1:n.-49C>T
ENST00000337432.8:c.-49C>T	ENSP00000336701.4:n.-49C>T
ENST00000461271.5:c.-297C>T	ENSP00000464056.1:n.-297C>T
ENST00000487921.5:n.20C>T
ENST00000583539.5:c.-49C>T	ENSP00000463121.1:n.-49C>T
NM_002876.3:c.-49C>T	NP_002867.1:n.-49C>T
NM_058216.2:c.-49C>T	NP_478123.1:n.-49C>T
NR_103872.1:n.23C>T
NR_103873.1:n.23C>T
XM_006722001.2:c.-49C>T	XP_006722064.1:n.-49C>T
XM_006722002.2:c.-49C>T	XP_006722065.1:n.-49C>T
XM_006722004.2:c.-297C>T	XP_006722067.1:n.-297C>T
XM_006722005.2:c.-244C>T	XP_006722068.1:n.-244C>T
XM_011525092.1:c.-597C>T	XP_011523394.1:n.-597C>T
XM_011525093.1:c.-758C>T	XP_011523395.1:n.-758C>T
XR_934513.1:n.25C>T
XR_934514.1:n.25C>T
XM_006722001.4:c.-49C>T	XP_006722064.1:n.-49C>T
XM_006722002.4:c.-49C>T	XP_006722065.1:n.-49C>T
XM_006722004.3:c.-297C>T	XP_006722067.1:n.-297C>T
XM_006722005.3:c.-244C>T	XP_006722068.1:n.-244C>T
XM_017024914.1:c.-297C>T	XP_016880403.1:n.-297C>T
XM_017024917.1:c.-244C>T	XP_016880406.1:n.-244C>T
XR_934513.3:n.456C>T
XR_934514.3:n.456C>T