Canonical Allele Identifier: CA773571819
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs1387810975
gnomAD v3: 17-58692537-C-T
gnomAD v4: 17-58692537-C-T
MyVariant Identifiers: chr17:g.56769898C>T (hg19) chr17:g.58692537C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692537C>T , CM000679.2:g.58692537C>T GRCh38
NC_000017.10:g.56769898C>T , CM000679.1:g.56769898C>T GRCh37
NC_000017.9:g.54124897C>T NCBI36
NG_023199.1:g.4936C>T , LRG_314:g.4936C>T
NG_047169.1:g.4543G>A

Transcript Alleles

HGVS Amino-acid change
XM_006722005.2:c.-302C>T XP_006722068.1:n.-302C>T
XM_006722001.4:c.-107C>T XP_006722064.1:n.-107C>T
XM_006722002.4:c.-107C>T XP_006722065.1:n.-107C>T
XR_934513.3:n.398C>T
XR_934514.3:n.398C>T
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