Canonical Allele Identifier: CA2267813869
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692532T= , CM000679.2:g.58692532T= GRCh38
NC_000017.10:g.56769893T= , CM000679.1:g.56769893T= GRCh37
NC_000017.9:g.54124892T= NCBI36
NG_023199.1:g.4931T= , LRG_314:g.4931T=
NG_047169.1:g.4548A=

Transcript Alleles

HGVS Amino-acid change
XM_006722001.4:c.-112T= XP_006722064.1:n.-112T=
XM_006722002.4:c.-112T= XP_006722065.1:n.-112T=
XR_934513.3:n.393T=
XR_934514.3:n.393T=