Canonical Allele Identifier: CA627144479
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs1332499205
gnomAD v2: 17-56769824-T-A
gnomAD v3: 17-58692463-T-A
gnomAD v4: 17-58692463-T-A
MyVariant Identifiers: chr17:g.56769824T>A (hg19) chr17:g.58692463T>A (hg38)
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Genomic Alleles

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

Transcript Alleles

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