Canonical Allele Identifier: CA602632029

Gene: RAD52

Linked Data

• dbSNP Id: rs1318786314
• gnomAD v2: 12-1064521-C-T
• gnomAD v3: 12-955355-C-T
• gnomAD v4: 12-955355-C-T
• MyVariant Identifiers: chr12:g.1064521C>T (hg19) ; chr12:g.955355C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.955355C>T , CM000674.2:g.955355C>T	GRCh38
NC_000012.11:g.1064521C>T , CM000674.1:g.1064521C>T	GRCh37
NC_000012.10:g.934782C>T	NCBI36
NG_017078.2:g.39687G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000430095.6:c.-18-22279G>A	ENSP00000387901.2:n.-18-22279G>A
NM_001297419.1:c.-18-22279G>A	NP_001284348.1:n.-18-22279G>A
XM_005253720.3:c.-18-22279G>A	XP_005253777.1:n.-18-22279G>A
XM_005253720.5:c.-18-22279G>A	XP_005253777.1:n.-18-22279G>A
XM_017019769.1:c.-18-22279G>A	XP_016875258.1:n.-18-22279G>A