Canonical Allele Identifier: CA773571720
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs1332499205
MyVariant Identifiers: chr17:g.56769824T>C (hg19) chr17:g.58692463T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692463T>C , CM000679.2:g.58692463T>C GRCh38
NC_000017.10:g.56769824T>C , CM000679.1:g.56769824T>C GRCh37
NC_000017.9:g.54124823T>C NCBI36
NG_023199.1:g.4862T>C , LRG_314:g.4862T>C
NG_047169.1:g.4617A>G

Transcript Alleles

HGVS Amino-acid change
XM_006722001.4:c.-181T>C XP_006722064.1:n.-181T>C
XM_006722002.4:c.-181T>C XP_006722065.1:n.-181T>C
XR_934513.3:n.324T>C
XR_934514.3:n.324T>C
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