Canonical Allele Identifier: CA2267813791
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs2047779650
gnomAD v4: 17-58692432-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692432A>T , CM000679.2:g.58692432A>T GRCh38
NC_000017.10:g.56769793A>T , CM000679.1:g.56769793A>T GRCh37
NC_000017.9:g.54124792A>T NCBI36
NG_023199.1:g.4831A>T , LRG_314:g.4831A>T
NG_047169.1:g.4648T>A

Transcript Alleles

HGVS Amino-acid change
XM_006722001.4:c.-212A>T XP_006722064.1:n.-212A>T
XM_006722002.4:c.-212A>T XP_006722065.1:n.-212A>T
XR_934513.3:n.293A>T
XR_934514.3:n.293A>T
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