Canonical Allele Identifier: CA2267813898
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692568C= , CM000679.2:g.58692568C= GRCh38
NC_000017.10:g.56769929C= , CM000679.1:g.56769929C= GRCh37
NC_000017.9:g.54124928C= NCBI36
NG_023199.1:g.4967C= , LRG_314:g.4967C=
NG_047169.1:g.4512G=

Transcript Alleles

HGVS Amino-acid Change
XM_006722005.2:c.-271C= XP_006722068.1:n.-271C=
XM_006722001.4:c.-76C= XP_006722064.1:n.-76C=
XM_006722002.4:c.-76C= XP_006722065.1:n.-76C=
XM_006722005.3:c.-271C= XP_006722068.1:n.-271C=
XM_017024917.1:c.-271C= XP_016880406.1:n.-271C=
XR_934513.3:n.429C=
XR_934514.3:n.429C=