Canonical Allele Identifier: CA2638988528
Gene: RAD51C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692547G>T , CM000679.2:g.58692547G>T GRCh38
NC_000017.10:g.56769908G>T , CM000679.1:g.56769908G>T GRCh37
NC_000017.9:g.54124907G>T NCBI36
NG_023199.1:g.4946G>T , LRG_314:g.4946G>T
NG_047169.1:g.4533C>A

Transcript Alleles

HGVS Amino-acid change
XM_006722005.2:c.-292G>T XP_006722068.1:n.-292G>T
XM_006722001.4:c.-97G>T XP_006722064.1:n.-97G>T
XM_006722002.4:c.-97G>T XP_006722065.1:n.-97G>T
XM_006722005.3:c.-292G>T XP_006722068.1:n.-292G>T
XM_017024917.1:c.-292G>T XP_016880406.1:n.-292G>T
XR_934513.3:n.408G>T
XR_934514.3:n.408G>T