Canonical Allele Identifier: CA2011752897
Gene: RAD52 HGNC NCBI

Linked Data

dbSNP Id: rs10774474

Genomic Alleles

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

Transcript Alleles

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