Canonical Allele Identifier: CA2011754837
Gene: RAD52 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.955253G= , CM000674.2:g.955253G= GRCh38
NC_000012.11:g.1064419G= , CM000674.1:g.1064419G= GRCh37
NC_000012.10:g.934680G= NCBI36
NG_017078.2:g.39789C=

Transcript Alleles

HGVS Amino-acid change
ENST00000430095.6:c.-18-22177C= ENSP00000387901.2:n.-18-22177C=
NM_001297419.1:c.-18-22177C= NP_001284348.1:n.-18-22177C=
XM_005253720.3:c.-18-22177C= XP_005253777.1:n.-18-22177C=
XM_005253720.5:c.-18-22177C= XP_005253777.1:n.-18-22177C=
XM_017019769.1:c.-18-22177C= XP_016875258.1:n.-18-22177C=