Canonical Allele Identifier: CA2267813862
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs189059313
gnomAD v4: 17-58692527-C-G
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Genomic Alleles

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

Transcript Alleles

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