Canonical Allele Identifier: CA2809980335
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692566T>G , CM000679.2:g.58692566T>G GRCh38
NC_000017.10:g.56769927T>G , CM000679.1:g.56769927T>G GRCh37
NC_000017.9:g.54124926T>G NCBI36
NG_023199.1:g.4965T>G , LRG_314:g.4965T>G
NG_047169.1:g.4514A>C

Transcript Alleles

HGVS Amino-acid Change
XM_006722005.2:c.-273T>G XP_006722068.1:n.-273T>G
XM_006722001.4:c.-78T>G XP_006722064.1:n.-78T>G
XM_006722002.4:c.-78T>G XP_006722065.1:n.-78T>G
XM_006722005.3:c.-273T>G XP_006722068.1:n.-273T>G
XM_017024917.1:c.-273T>G XP_016880406.1:n.-273T>G
XR_934513.3:n.427T>G
XR_934514.3:n.427T>G