Canonical Allele Identifier: CA2011754836
Gene: RAD52 HGNC NCBI

Linked Data

dbSNP Id: rs1958588344

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.955252G>A , CM000674.2:g.955252G>A GRCh38
NC_000012.11:g.1064418G>A , CM000674.1:g.1064418G>A GRCh37
NC_000012.10:g.934679G>A NCBI36
NG_017078.2:g.39790C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000430095.6:c.-18-22176C>T ENSP00000387901.2:n.-18-22176C>T
NM_001297419.1:c.-18-22176C>T NP_001284348.1:n.-18-22176C>T
XM_005253720.3:c.-18-22176C>T XP_005253777.1:n.-18-22176C>T
XM_005253720.5:c.-18-22176C>T XP_005253777.1:n.-18-22176C>T
XM_017019769.1:c.-18-22176C>T XP_016875258.1:n.-18-22176C>T