Canonical Allele Identifier: CA292046461
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs929669006
gnomAD v3: 17-58692525-A-C
gnomAD v4: 17-58692525-A-C
MyVariant Identifiers: chr17:g.56769886A>C (hg19) chr17:g.58692525A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692525A>C , CM000679.2:g.58692525A>C GRCh38
NC_000017.10:g.56769886A>C , CM000679.1:g.56769886A>C GRCh37
NC_000017.9:g.54124885A>C NCBI36
NG_023199.1:g.4924A>C , LRG_314:g.4924A>C
NG_047169.1:g.4555T>G

Transcript Alleles

HGVS Amino-acid change
XM_006722001.4:c.-119A>C XP_006722064.1:n.-119A>C
XM_006722002.4:c.-119A>C XP_006722065.1:n.-119A>C
XR_934513.3:n.386A>C
XR_934514.3:n.386A>C
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