Canonical Allele Identifier: CA2638988579
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs892464609

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692562G>C , CM000679.2:g.58692562G>C GRCh38
NC_000017.10:g.56769923G>C , CM000679.1:g.56769923G>C GRCh37
NC_000017.9:g.54124922G>C NCBI36
NG_023199.1:g.4961G>C , LRG_314:g.4961G>C
NG_047169.1:g.4518C>G

Transcript Alleles

HGVS Amino-acid change
XM_006722005.2:c.-277G>C XP_006722068.1:n.-277G>C
XM_006722001.4:c.-82G>C XP_006722064.1:n.-82G>C
XM_006722002.4:c.-82G>C XP_006722065.1:n.-82G>C
XM_006722005.3:c.-277G>C XP_006722068.1:n.-277G>C
XM_017024917.1:c.-277G>C XP_016880406.1:n.-277G>C
XR_934513.3:n.423G>C
XR_934514.3:n.423G>C