Canonical Allele Identifier: CA2638988602
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs2047788481

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692574A>G , CM000679.2:g.58692574A>G GRCh38
NC_000017.10:g.56769935A>G , CM000679.1:g.56769935A>G GRCh37
NC_000017.9:g.54124934A>G NCBI36
NG_023199.1:g.4973A>G , LRG_314:g.4973A>G
NG_047169.1:g.4506T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000461271.6:c.-318A>G ENSP00000464056.2:n.-318A>G
ENST00000697675.1:n.2A>G
ENST00000337432.8:c.-70A>G ENSP00000336701.4:n.-70A>G
ENST00000461271.5:c.-318A>G ENSP00000464056.1:n.-318A>G
ENST00000583539.5:c.-70A>G ENSP00000463121.1:n.-70A>G
NM_002876.3:c.-70A>G NP_002867.1:n.-70A>G
NM_058216.2:c.-70A>G NP_478123.1:n.-70A>G
NR_103872.1:n.2A>G
NR_103873.1:n.2A>G
XM_006722001.2:c.-70A>G XP_006722064.1:n.-70A>G
XM_006722002.2:c.-70A>G XP_006722065.1:n.-70A>G
XM_006722005.2:c.-265A>G XP_006722068.1:n.-265A>G
XR_934513.1:n.4A>G
XR_934514.1:n.4A>G
XM_006722001.4:c.-70A>G XP_006722064.1:n.-70A>G
XM_006722002.4:c.-70A>G XP_006722065.1:n.-70A>G
XM_006722005.3:c.-265A>G XP_006722068.1:n.-265A>G
XM_017024917.1:c.-265A>G XP_016880406.1:n.-265A>G
XR_934513.3:n.435A>G
XR_934514.3:n.435A>G