Canonical Allele Identifier: CA2638988653
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs2143667287

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692585C>A , CM000679.2:g.58692585C>A GRCh38
NC_000017.10:g.56769946C>A , CM000679.1:g.56769946C>A GRCh37
NC_000017.9:g.54124945C>A NCBI36
NG_023199.1:g.4984C>A , LRG_314:g.4984C>A
NG_047169.1:g.4495G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.-307C>A ENSP00000464056.2:n.-307C>A
ENST00000697675.1:n.13C>A
ENST00000697676.1:n.2C>A
ENST00000697683.1:c.-59C>A ENSP00000513395.1:n.-59C>A
ENST00000697684.1:n.2C>A
ENST00000337432.8:c.-59C>A ENSP00000336701.4:n.-59C>A
ENST00000461271.5:c.-307C>A ENSP00000464056.1:n.-307C>A
ENST00000487921.5:n.10C>A
ENST00000583539.5:c.-59C>A ENSP00000463121.1:n.-59C>A
NM_002876.3:c.-59C>A NP_002867.1:n.-59C>A
NM_058216.2:c.-59C>A NP_478123.1:n.-59C>A
NR_103872.1:n.13C>A
NR_103873.1:n.13C>A
XM_006722001.2:c.-59C>A XP_006722064.1:n.-59C>A
XM_006722002.2:c.-59C>A XP_006722065.1:n.-59C>A
XM_006722004.2:c.-307C>A XP_006722067.1:n.-307C>A
XM_006722005.2:c.-254C>A XP_006722068.1:n.-254C>A
XR_934513.1:n.15C>A
XR_934514.1:n.15C>A
XM_006722001.4:c.-59C>A XP_006722064.1:n.-59C>A
XM_006722002.4:c.-59C>A XP_006722065.1:n.-59C>A
XM_006722004.3:c.-307C>A XP_006722067.1:n.-307C>A
XM_006722005.3:c.-254C>A XP_006722068.1:n.-254C>A
XM_017024914.1:c.-307C>A XP_016880403.1:n.-307C>A
XM_017024917.1:c.-254C>A XP_016880406.1:n.-254C>A
XR_934513.3:n.446C>A
XR_934514.3:n.446C>A