Canonical Allele Identifier: CA2011754825
Gene: RAD52 HGNC NCBI

Linked Data

dbSNP Id: rs1958588111

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.955237T>C , CM000674.2:g.955237T>C GRCh38
NC_000012.11:g.1064403T>C , CM000674.1:g.1064403T>C GRCh37
NC_000012.10:g.934664T>C NCBI36
NG_017078.2:g.39805A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000430095.6:c.-18-22161A>G ENSP00000387901.2:n.-18-22161A>G
NM_001297419.1:c.-18-22161A>G NP_001284348.1:n.-18-22161A>G
XM_005253720.3:c.-18-22161A>G XP_005253777.1:n.-18-22161A>G
XM_005253720.5:c.-18-22161A>G XP_005253777.1:n.-18-22161A>G
XM_017019769.1:c.-18-22161A>G XP_016875258.1:n.-18-22161A>G