Canonical Allele Identifier: CA231500247
Gene: RAD52 HGNC NCBI

Linked Data

dbSNP Id: rs944071238
gnomAD v3: 12-955173-T-A
gnomAD v4: 12-955173-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.955173T>A , CM000674.2:g.955173T>A GRCh38
NC_000012.11:g.1064339T>A , CM000674.1:g.1064339T>A GRCh37
NC_000012.10:g.934600T>A NCBI36
NG_017078.2:g.39869A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000430095.6:c.-18-22097A>T ENSP00000387901.2:n.-18-22097A>T
NM_001297419.1:c.-18-22097A>T NP_001284348.1:n.-18-22097A>T
XM_005253720.3:c.-18-22097A>T XP_005253777.1:n.-18-22097A>T
XM_005253720.5:c.-18-22097A>T XP_005253777.1:n.-18-22097A>T
XM_017019769.1:c.-18-22097A>T XP_016875258.1:n.-18-22097A>T