Canonical Allele Identifier: CA231500259
Gene: RAD52 HGNC NCBI

Linked Data

dbSNP Id: rs897283343

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.955213A>G , CM000674.2:g.955213A>G GRCh38
NC_000012.11:g.1064379A>G , CM000674.1:g.1064379A>G GRCh37
NC_000012.10:g.934640A>G NCBI36
NG_017078.2:g.39829T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000430095.6:c.-18-22137T>C ENSP00000387901.2:n.-18-22137T>C
NM_001297419.1:c.-18-22137T>C NP_001284348.1:n.-18-22137T>C
XM_005253720.3:c.-18-22137T>C XP_005253777.1:n.-18-22137T>C
XM_005253720.5:c.-18-22137T>C XP_005253777.1:n.-18-22137T>C
XM_017019769.1:c.-18-22137T>C XP_016875258.1:n.-18-22137T>C