Canonical Allele Identifier: CA292046412
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs958815453
gnomAD v4: 17-58692450-G-T
MyVariant Identifiers: chr17:g.56769811G>T (hg19) chr17:g.58692450G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692450G>T , CM000679.2:g.58692450G>T GRCh38
NC_000017.10:g.56769811G>T , CM000679.1:g.56769811G>T GRCh37
NC_000017.9:g.54124810G>T NCBI36
NG_023199.1:g.4849G>T , LRG_314:g.4849G>T
NG_047169.1:g.4630C>A

Transcript Alleles

HGVS Amino-acid Change
XM_006722001.4:c.-194G>T XP_006722064.1:n.-194G>T
XM_006722002.4:c.-194G>T XP_006722065.1:n.-194G>T
XR_934513.3:n.311G>T
XR_934514.3:n.311G>T
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