Canonical Allele Identifier: CA13771537

Gene: RAD52

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.963799C>T , CM000674.2:g.963799C>T	GRCh38
NC_000012.11:g.1072965C>T , CM000674.1:g.1072965C>T	GRCh37
NC_000012.10:g.943226C>T	NCBI36
NG_017078.2:g.31243G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430095.6:c.-19+26010G>A	ENSP00000387901.2:n.-19+26010G>A
NM_001297419.1:c.-19+26010G>A	NP_001284348.1:n.-19+26010G>A
XM_005253720.3:c.-19+26010G>A	XP_005253777.1:n.-19+26010G>A
XM_005253720.5:c.-19+26010G>A	XP_005253777.1:n.-19+26010G>A
XM_017019769.1:c.-19+26010G>A	XP_016875258.1:n.-19+26010G>A