Canonical Allele Identifier: CA2733773171
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs2143666519

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692572_58692578del , CM000679.2:g.58692572_58692578del GRCh38
NC_000017.10:g.56769933_56769939del , CM000679.1:g.56769933_56769939del GRCh37
NC_000017.9:g.54124932_54124938del NCBI36
NG_023199.1:g.4971_4977del , LRG_314:g.4971_4977del
NG_047169.1:g.4507_4513del

Transcript Alleles

HGVS Amino-acid Change
XM_006722005.2:c.-267_-261del XP_006722068.1:n.-267_-261del
XM_006722001.4:c.-72_-66del XP_006722064.1:n.-72_-66del
XM_006722002.4:c.-72_-66del XP_006722065.1:n.-72_-66del
XM_006722005.3:c.-267_-261del XP_006722068.1:n.-267_-261del
XM_017024917.1:c.-267_-261del XP_016880406.1:n.-267_-261del
XR_934513.3:n.433_439del
XR_934514.3:n.433_439del