Canonical Allele Identifier: CA693750105
Gene: RAD52 HGNC NCBI

Linked Data

dbSNP Id: rs1193940668

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.955200G>A , CM000674.2:g.955200G>A GRCh38
NC_000012.11:g.1064366G>A , CM000674.1:g.1064366G>A GRCh37
NC_000012.10:g.934627G>A NCBI36
NG_017078.2:g.39842C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000430095.6:c.-18-22124C>T ENSP00000387901.2:n.-18-22124C>T
NM_001297419.1:c.-18-22124C>T NP_001284348.1:n.-18-22124C>T
XM_005253720.3:c.-18-22124C>T XP_005253777.1:n.-18-22124C>T
XM_005253720.5:c.-18-22124C>T XP_005253777.1:n.-18-22124C>T
XM_017019769.1:c.-18-22124C>T XP_016875258.1:n.-18-22124C>T