Canonical Allele Identifier: CA2267813899
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692571C= , CM000679.2:g.58692571C= GRCh38
NC_000017.10:g.56769932C= , CM000679.1:g.56769932C= GRCh37
NC_000017.9:g.54124931C= NCBI36
NG_023199.1:g.4970C= , LRG_314:g.4970C=
NG_047169.1:g.4509G=

Transcript Alleles

HGVS Amino-acid Change
XM_006722001.2:c.-73C= XP_006722064.1:n.-73C=
XM_006722002.2:c.-73C= XP_006722065.1:n.-73C=
XM_006722005.2:c.-268C= XP_006722068.1:n.-268C=
XR_934513.1:n.1C=
XR_934514.1:n.1C=
XM_006722001.4:c.-73C= XP_006722064.1:n.-73C=
XM_006722002.4:c.-73C= XP_006722065.1:n.-73C=
XM_006722005.3:c.-268C= XP_006722068.1:n.-268C=
XM_017024917.1:c.-268C= XP_016880406.1:n.-268C=
XR_934513.3:n.432C=
XR_934514.3:n.432C=