Canonical Allele Identifier: CA2011754883
Gene: RAD52 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.955372C= , CM000674.2:g.955372C= GRCh38
NC_000012.11:g.1064538C= , CM000674.1:g.1064538C= GRCh37
NC_000012.10:g.934799C= NCBI36
NG_017078.2:g.39670G=

Transcript Alleles

HGVS Amino-acid change
ENST00000430095.6:c.-18-22296G= ENSP00000387901.2:n.-18-22296G=
NM_001297419.1:c.-18-22296G= NP_001284348.1:n.-18-22296G=
XM_005253720.3:c.-18-22296G= XP_005253777.1:n.-18-22296G=
XM_005253720.5:c.-18-22296G= XP_005253777.1:n.-18-22296G=
XM_017019769.1:c.-18-22296G= XP_016875258.1:n.-18-22296G=