Canonical Allele Identifier: CA626733409
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs1348129934
gnomAD v2: 17-56769696-C-T
gnomAD v3: 17-58692335-C-T
gnomAD v4: 17-58692335-C-T
MyVariant Identifiers: chr17:g.56769696C>T (hg19) chr17:g.58692335C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692335C>T , CM000679.2:g.58692335C>T GRCh38
NC_000017.10:g.56769696C>T , CM000679.1:g.56769696C>T GRCh37
NC_000017.9:g.54124695C>T NCBI36
NG_023199.1:g.4734C>T , LRG_314:g.4734C>T
NG_047169.1:g.4745G>A

Transcript Alleles

HGVS Amino-acid Change
XM_006722001.4:c.-309C>T XP_006722064.1:n.-309C>T
XM_006722002.4:c.-309C>T XP_006722065.1:n.-309C>T
XR_934513.3:n.196C>T
XR_934514.3:n.196C>T
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