Canonical Allele Identifier: CA2267813881
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692548A= , CM000679.2:g.58692548A= GRCh38
NC_000017.10:g.56769909A= , CM000679.1:g.56769909A= GRCh37
NC_000017.9:g.54124908A= NCBI36
NG_023199.1:g.4947A= , LRG_314:g.4947A=
NG_047169.1:g.4532T=

Transcript Alleles

HGVS Amino-acid change
XM_006722005.2:c.-291A= XP_006722068.1:n.-291A=
XM_006722001.4:c.-96A= XP_006722064.1:n.-96A=
XM_006722002.4:c.-96A= XP_006722065.1:n.-96A=
XM_006722005.3:c.-291A= XP_006722068.1:n.-291A=
XM_017024917.1:c.-291A= XP_016880406.1:n.-291A=
XR_934513.3:n.409A=
XR_934514.3:n.409A=