Canonical Allele Identifier: CA292046515
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 803439
ClinVar RCV Id: RCV000989954
dbSNP Id: rs545213879
gnomAD v2: 17-56769902-G-A
gnomAD v3: 17-58692541-G-A
gnomAD v4: 17-58692541-G-A
MyVariant Identifiers: chr17:g.56769902G>A (hg19) chr17:g.58692541G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692541G>A , CM000679.2:g.58692541G>A GRCh38
NC_000017.10:g.56769902G>A , CM000679.1:g.56769902G>A GRCh37
NC_000017.9:g.54124901G>A NCBI36
NG_023199.1:g.4940G>A , LRG_314:g.4940G>A
NG_047169.1:g.4539C>T

Transcript Alleles

HGVS Amino-acid change
XM_006722005.2:c.-298G>A XP_006722068.1:n.-298G>A
XM_006722001.4:c.-103G>A XP_006722064.1:n.-103G>A
XM_006722002.4:c.-103G>A XP_006722065.1:n.-103G>A
XM_006722005.3:c.-298G>A XP_006722068.1:n.-298G>A
XM_017024917.1:c.-298G>A XP_016880406.1:n.-298G>A
XR_934513.3:n.402G>A
XR_934514.3:n.402G>A
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