Canonical Allele Identifier: CA2267813794
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs2047779816

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692440T>C , CM000679.2:g.58692440T>C GRCh38
NC_000017.10:g.56769801T>C , CM000679.1:g.56769801T>C GRCh37
NC_000017.9:g.54124800T>C NCBI36
NG_023199.1:g.4839T>C , LRG_314:g.4839T>C
NG_047169.1:g.4640A>G

Transcript Alleles

HGVS Amino-acid change
XM_006722001.4:c.-204T>C XP_006722064.1:n.-204T>C
XM_006722002.4:c.-204T>C XP_006722065.1:n.-204T>C
XR_934513.3:n.301T>C
XR_934514.3:n.301T>C