Canonical Allele Identifier: CA16434142
Gene: RAD52 HGNC NCBI
MyVariant.info:
GRCh38 chr12:g.955272T>C
GRCh37 chr12:g.1064438T>C
gnomAD v2:
12:1064438 T / C
gnomAD v3:
12:955272 T / C
gnomAD v4:
chr12-955272-T-C
Joint Max Group AF 0.52214145 (NFE)
Genomes Max Group AF 0.52214145 (NFE)
dbSNP:
10849605
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.955272T>C , CM000674.2:g.955272T>C GRCh38
NC_000012.11:g.1064438T>C , CM000674.1:g.1064438T>C GRCh37
NC_000012.10:g.934699T>C NCBI36
NG_017078.2:g.39770A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000430095.6:c.-18-22196A>G ENSP00000387901.2:n.-18-22196A>G
NM_001297419.1:c.-18-22196A>G NP_001284348.1:n.-18-22196A>G
XM_005253720.3:c.-18-22196A>G XP_005253777.1:n.-18-22196A>G
XM_005253720.5:c.-18-22196A>G XP_005253777.1:n.-18-22196A>G
XM_017019769.1:c.-18-22196A>G XP_016875258.1:n.-18-22196A>G
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