Canonical Allele Identifier: CA231497601
Gene: RAD52 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.951120A>T , CM000674.2:g.951120A>T GRCh38
NC_000012.11:g.1060286A>T , CM000674.1:g.1060286A>T GRCh37
NC_000012.10:g.930547A>T NCBI36
NG_017078.1:g.3578T>A
NG_017078.2:g.43922T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000430095.6:c.-18-18044T>A ENSP00000387901.2:n.-18-18044T>A
NM_001297419.1:c.-18-18044T>A NP_001284348.1:n.-18-18044T>A
XM_005253720.3:c.-18-18044T>A XP_005253777.1:n.-18-18044T>A
XM_005253720.5:c.-18-18044T>A XP_005253777.1:n.-18-18044T>A
XM_017019769.1:c.-18-18044T>A XP_016875258.1:n.-18-18044T>A