Canonical Allele Identifier: CA693750104
Gene: RAD52 HGNC NCBI

Linked Data

dbSNP Id: rs1396507682
gnomAD v4: 12-955199-TG-T
MyVariant Identifiers: chr12:g.1064366del (hg19) chr12:g.955200del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.955202del , CM000674.2:g.955202del GRCh38
NC_000012.11:g.1064368del , CM000674.1:g.1064368del GRCh37
NC_000012.10:g.934629del NCBI36
NG_017078.2:g.39842del

Transcript Alleles

HGVS Amino-acid change
ENST00000430095.6:c.-18-22124del ENSP00000387901.2:n.-18-22124del
NM_001297419.1:c.-18-22124del NP_001284348.1:n.-18-22124del
XM_005253720.3:c.-18-22124del XP_005253777.1:n.-18-22124del
XM_005253720.5:c.-18-22124del XP_005253777.1:n.-18-22124del
XM_017019769.1:c.-18-22124del XP_016875258.1:n.-18-22124del
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