Canonical Allele Identifier: CA693750114

Gene: RAD52

Linked Data

• dbSNP Id: rs1228006662
• gnomAD v3: 12-955266-T-A
• gnomAD v4: 12-955266-T-A
• MyVariant Identifiers: chr12:g.1064432T>A (hg19) ; chr12:g.955266T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.955266T>A , CM000674.2:g.955266T>A	GRCh38
NC_000012.11:g.1064432T>A , CM000674.1:g.1064432T>A	GRCh37
NC_000012.10:g.934693T>A	NCBI36
NG_017078.2:g.39776A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000430095.6:c.-18-22190A>T	ENSP00000387901.2:n.-18-22190A>T
NM_001297419.1:c.-18-22190A>T	NP_001284348.1:n.-18-22190A>T
XM_005253720.3:c.-18-22190A>T	XP_005253777.1:n.-18-22190A>T
XM_005253720.5:c.-18-22190A>T	XP_005253777.1:n.-18-22190A>T
XM_017019769.1:c.-18-22190A>T	XP_016875258.1:n.-18-22190A>T