Canonical Allele Identifier: CA2267813880
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs2047787020
gnomAD v4: 17-58692546-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692546A>G , CM000679.2:g.58692546A>G GRCh38
NC_000017.10:g.56769907A>G , CM000679.1:g.56769907A>G GRCh37
NC_000017.9:g.54124906A>G NCBI36
NG_023199.1:g.4945A>G , LRG_314:g.4945A>G
NG_047169.1:g.4534T>C

Transcript Alleles

HGVS Amino-acid change
XM_006722005.2:c.-293A>G XP_006722068.1:n.-293A>G
XM_006722001.4:c.-98A>G XP_006722064.1:n.-98A>G
XM_006722002.4:c.-98A>G XP_006722065.1:n.-98A>G
XM_006722005.3:c.-293A>G XP_006722068.1:n.-293A>G
XM_017024917.1:c.-293A>G XP_016880406.1:n.-293A>G
XR_934513.3:n.407A>G
XR_934514.3:n.407A>G
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