Canonical Allele Identifier: CA985049538
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs1403887270
gnomAD v3: 17-58692534-C-T
gnomAD v4: 17-58692534-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692534C>T , CM000679.2:g.58692534C>T GRCh38
NC_000017.10:g.56769895C>T , CM000679.1:g.56769895C>T GRCh37
NC_000017.9:g.54124894C>T NCBI36
NG_023199.1:g.4933C>T , LRG_314:g.4933C>T
NG_047169.1:g.4546G>A

Transcript Alleles

HGVS Amino-acid change
XM_006722001.4:c.-110C>T XP_006722064.1:n.-110C>T
XM_006722002.4:c.-110C>T XP_006722065.1:n.-110C>T
XR_934513.3:n.395C>T
XR_934514.3:n.395C>T
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