Canonical Allele Identifier: CA292046516
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs893449142
gnomAD v4: 17-58692542-C-A
MyVariant Identifiers: chr17:g.56769903C>A (hg19) chr17:g.58692542C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692542C>A , CM000679.2:g.58692542C>A GRCh38
NC_000017.10:g.56769903C>A , CM000679.1:g.56769903C>A GRCh37
NC_000017.9:g.54124902C>A NCBI36
NG_023199.1:g.4941C>A , LRG_314:g.4941C>A
NG_047169.1:g.4538G>T

Transcript Alleles

HGVS Amino-acid change
XM_006722005.2:c.-297C>A XP_006722068.1:n.-297C>A
XM_006722001.4:c.-102C>A XP_006722064.1:n.-102C>A
XM_006722002.4:c.-102C>A XP_006722065.1:n.-102C>A
XM_006722005.3:c.-297C>A XP_006722068.1:n.-297C>A
XM_017024917.1:c.-297C>A XP_016880406.1:n.-297C>A
XR_934513.3:n.403C>A
XR_934514.3:n.403C>A
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