Canonical Allele Identifier: CA943969578
Gene: RAD52 HGNC NCBI

Linked Data

dbSNP Id: rs1958589907
gnomAD v3: 12-955375-T-C
gnomAD v4: 12-955375-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.955375T>C , CM000674.2:g.955375T>C GRCh38
NC_000012.11:g.1064541T>C , CM000674.1:g.1064541T>C GRCh37
NC_000012.10:g.934802T>C NCBI36
NG_017078.2:g.39667A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000430095.6:c.-18-22299A>G ENSP00000387901.2:n.-18-22299A>G
NM_001297419.1:c.-18-22299A>G NP_001284348.1:n.-18-22299A>G
XM_005253720.3:c.-18-22299A>G XP_005253777.1:n.-18-22299A>G
XM_005253720.5:c.-18-22299A>G XP_005253777.1:n.-18-22299A>G
XM_017019769.1:c.-18-22299A>G XP_016875258.1:n.-18-22299A>G