Canonical Allele Identifier: CA2733773636
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs2143667170

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692584G>C , CM000679.2:g.58692584G>C GRCh38
NC_000017.10:g.56769945G>C , CM000679.1:g.56769945G>C GRCh37
NC_000017.9:g.54124944G>C NCBI36
NG_023199.1:g.4983G>C , LRG_314:g.4983G>C
NG_047169.1:g.4496C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000461271.6:c.-308G>C ENSP00000464056.2:n.-308G>C
ENST00000697675.1:n.12G>C
ENST00000697676.1:n.1G>C
ENST00000697683.1:c.-60G>C ENSP00000513395.1:n.-60G>C
ENST00000697684.1:n.1G>C
ENST00000337432.8:c.-60G>C ENSP00000336701.4:n.-60G>C
ENST00000461271.5:c.-308G>C ENSP00000464056.1:n.-308G>C
ENST00000487921.5:n.9G>C
ENST00000583539.5:c.-60G>C ENSP00000463121.1:n.-60G>C
NM_002876.3:c.-60G>C NP_002867.1:n.-60G>C
NM_058216.2:c.-60G>C NP_478123.1:n.-60G>C
NR_103872.1:n.12G>C
NR_103873.1:n.12G>C
XM_006722001.2:c.-60G>C XP_006722064.1:n.-60G>C
XM_006722002.2:c.-60G>C XP_006722065.1:n.-60G>C
XM_006722004.2:c.-308G>C XP_006722067.1:n.-308G>C
XM_006722005.2:c.-255G>C XP_006722068.1:n.-255G>C
XR_934513.1:n.14G>C
XR_934514.1:n.14G>C
XM_006722001.4:c.-60G>C XP_006722064.1:n.-60G>C
XM_006722002.4:c.-60G>C XP_006722065.1:n.-60G>C
XM_006722004.3:c.-308G>C XP_006722067.1:n.-308G>C
XM_006722005.3:c.-255G>C XP_006722068.1:n.-255G>C
XM_017024914.1:c.-308G>C XP_016880403.1:n.-308G>C
XM_017024917.1:c.-255G>C XP_016880406.1:n.-255G>C
XR_934513.3:n.445G>C
XR_934514.3:n.445G>C