Canonical Allele Identifier: CA2011754819
Gene: RAD52 HGNC NCBI

Linked Data

dbSNP Id: rs1958587888
gnomAD v3: 12-955227-C-T
gnomAD v4: 12-955227-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.955227C>T , CM000674.2:g.955227C>T GRCh38
NC_000012.11:g.1064393C>T , CM000674.1:g.1064393C>T GRCh37
NC_000012.10:g.934654C>T NCBI36
NG_017078.2:g.39815G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000430095.6:c.-18-22151G>A ENSP00000387901.2:n.-18-22151G>A
NM_001297419.1:c.-18-22151G>A NP_001284348.1:n.-18-22151G>A
XM_005253720.3:c.-18-22151G>A XP_005253777.1:n.-18-22151G>A
XM_005253720.5:c.-18-22151G>A XP_005253777.1:n.-18-22151G>A
XM_017019769.1:c.-18-22151G>A XP_016875258.1:n.-18-22151G>A
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