Canonical Allele Identifier: CA2011754888
Gene: RAD52 HGNC NCBI

Linked Data

dbSNP Id: rs1958590024

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.955383dup , CM000674.2:g.955383dup GRCh38
NC_000012.11:g.1064549dup , CM000674.1:g.1064549dup GRCh37
NC_000012.10:g.934810dup NCBI36
NG_017078.2:g.39659dup

Transcript Alleles

HGVS Amino-acid change
ENST00000430095.6:c.-18-22307dup ENSP00000387901.2:n.-18-22307dup
NM_001297419.1:c.-18-22307dup NP_001284348.1:n.-18-22307dup
XM_005253720.3:c.-18-22307dup XP_005253777.1:n.-18-22307dup
XM_005253720.5:c.-18-22307dup XP_005253777.1:n.-18-22307dup
XM_017019769.1:c.-18-22307dup XP_016875258.1:n.-18-22307dup