Canonical Allele Identifier: CA693750106
Gene: RAD52 HGNC NCBI

Linked Data

dbSNP Id: rs1448330569
gnomAD v3: 12-955205-A-T
gnomAD v4: 12-955205-A-T
MyVariant Identifiers: chr12:g.1064371A>T (hg19) chr12:g.955205A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.955205A>T , CM000674.2:g.955205A>T GRCh38
NC_000012.11:g.1064371A>T , CM000674.1:g.1064371A>T GRCh37
NC_000012.10:g.934632A>T NCBI36
NG_017078.2:g.39837T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000430095.6:c.-18-22129T>A ENSP00000387901.2:n.-18-22129T>A
NM_001297419.1:c.-18-22129T>A NP_001284348.1:n.-18-22129T>A
XM_005253720.3:c.-18-22129T>A XP_005253777.1:n.-18-22129T>A
XM_005253720.5:c.-18-22129T>A XP_005253777.1:n.-18-22129T>A
XM_017019769.1:c.-18-22129T>A XP_016875258.1:n.-18-22129T>A
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