Canonical Allele Identifier: CA2638988514
Gene: RAD51C HGNC NCBI

Linked Data

gnomAD v4: 17-58692539-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692539A>C , CM000679.2:g.58692539A>C GRCh38
NC_000017.10:g.56769900A>C , CM000679.1:g.56769900A>C GRCh37
NC_000017.9:g.54124899A>C NCBI36
NG_023199.1:g.4938A>C , LRG_314:g.4938A>C
NG_047169.1:g.4541T>G

Transcript Alleles

HGVS Amino-acid change
XM_006722005.2:c.-300A>C XP_006722068.1:n.-300A>C
XM_006722001.4:c.-105A>C XP_006722064.1:n.-105A>C
XM_006722002.4:c.-105A>C XP_006722065.1:n.-105A>C
XM_006722005.3:c.-300A>C XP_006722068.1:n.-300A>C
XM_017024917.1:c.-300A>C XP_016880406.1:n.-300A>C
XR_934513.3:n.400A>C
XR_934514.3:n.400A>C
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