Canonical Allele Identifier: CA693750135

Gene: RAD52

Linked Data

• dbSNP Id: rs1186496300
• gnomAD v3: 12-955367-G-C
• gnomAD v4: 12-955367-G-C
• MyVariant Identifiers: chr12:g.1064533G>C (hg19) ; chr12:g.955367G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.955367G>C , CM000674.2:g.955367G>C	GRCh38
NC_000012.11:g.1064533G>C , CM000674.1:g.1064533G>C	GRCh37
NC_000012.10:g.934794G>C	NCBI36
NG_017078.2:g.39675C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000430095.6:c.-18-22291C>G	ENSP00000387901.2:n.-18-22291C>G
NM_001297419.1:c.-18-22291C>G	NP_001284348.1:n.-18-22291C>G
XM_005253720.3:c.-18-22291C>G	XP_005253777.1:n.-18-22291C>G
XM_005253720.5:c.-18-22291C>G	XP_005253777.1:n.-18-22291C>G
XM_017019769.1:c.-18-22291C>G	XP_016875258.1:n.-18-22291C>G