Canonical Allele Identifier: CA292046473
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs189059313

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692527C>T , CM000679.2:g.58692527C>T GRCh38
NC_000017.10:g.56769888C>T , CM000679.1:g.56769888C>T GRCh37
NC_000017.9:g.54124887C>T NCBI36
NG_023199.1:g.4926C>T , LRG_314:g.4926C>T
NG_047169.1:g.4553G>A

Transcript Alleles

HGVS Amino-acid change
XM_006722001.4:c.-117C>T XP_006722064.1:n.-117C>T
XM_006722002.4:c.-117C>T XP_006722065.1:n.-117C>T
XR_934513.3:n.388C>T
XR_934514.3:n.388C>T