Canonical Allele Identifier: CA292046629

Gene: RAD51C

Linked Data

• dbSNP Id: rs28363298
• gnomAD v4: 17-58692590-C-G
• MyVariant Identifiers: chr17:g.56769951C>G (hg19) ; chr17:g.58692590C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692590C>G , CM000679.2:g.58692590C>G	GRCh38
NC_000017.10:g.56769951C>G , CM000679.1:g.56769951C>G	GRCh37
NC_000017.9:g.54124950C>G	NCBI36
NG_023199.1:g.4989C>G , LRG_314:g.4989C>G
NG_047169.1:g.4490G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-302C>G	ENSP00000464056.2:n.-302C>G
ENST00000697675.1:n.18C>G
ENST00000697676.1:n.7C>G
ENST00000697677.1:n.5C>G
ENST00000697678.1:n.5C>G
ENST00000697683.1:c.-54C>G	ENSP00000513395.1:n.-54C>G
ENST00000697684.1:n.7C>G
ENST00000337432.8:c.-54C>G	ENSP00000336701.4:n.-54C>G
ENST00000461271.5:c.-302C>G	ENSP00000464056.1:n.-302C>G
ENST00000487921.5:n.15C>G
ENST00000583539.5:c.-54C>G	ENSP00000463121.1:n.-54C>G
NM_002876.3:c.-54C>G	NP_002867.1:n.-54C>G
NM_058216.2:c.-54C>G	NP_478123.1:n.-54C>G
NR_103872.1:n.18C>G
NR_103873.1:n.18C>G
XM_006722001.2:c.-54C>G	XP_006722064.1:n.-54C>G
XM_006722002.2:c.-54C>G	XP_006722065.1:n.-54C>G
XM_006722004.2:c.-302C>G	XP_006722067.1:n.-302C>G
XM_006722005.2:c.-249C>G	XP_006722068.1:n.-249C>G
XM_011525092.1:c.-602C>G	XP_011523394.1:n.-602C>G
XM_011525093.1:c.-763C>G	XP_011523395.1:n.-763C>G
XR_934513.1:n.20C>G
XR_934514.1:n.20C>G
XM_006722001.4:c.-54C>G	XP_006722064.1:n.-54C>G
XM_006722002.4:c.-54C>G	XP_006722065.1:n.-54C>G
XM_006722004.3:c.-302C>G	XP_006722067.1:n.-302C>G
XM_006722005.3:c.-249C>G	XP_006722068.1:n.-249C>G
XM_017024914.1:c.-302C>G	XP_016880403.1:n.-302C>G
XM_017024917.1:c.-249C>G	XP_016880406.1:n.-249C>G
XR_934513.3:n.451C>G
XR_934514.3:n.451C>G