Canonical Allele Identifier: CA773571754
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs1459620734
gnomAD v3: 17-58692483-AGT-A
gnomAD v4: 17-58692483-AGT-A
MyVariant Identifiers: chr17:g.56769845_56769846del (hg19) chr17:g.58692484_58692485del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692487_58692488del , CM000679.2:g.58692487_58692488del GRCh38
NC_000017.10:g.56769848_56769849del , CM000679.1:g.56769848_56769849del GRCh37
NC_000017.9:g.54124847_54124848del NCBI36
NG_023199.1:g.4886_4887del , LRG_314:g.4886_4887del
NG_047169.1:g.4595_4596del

Transcript Alleles

HGVS Amino-acid Change
XM_006722001.4:c.-157_-156del XP_006722064.1:n.-157_-156del
XM_006722002.4:c.-157_-156del XP_006722065.1:n.-157_-156del
XR_934513.3:n.348_349del
XR_934514.3:n.348_349del
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