Canonical Allele Identifier: CA585753473

Gene: UHRF2

Linked Data

• dbSNP Id: rs1285456103
• gnomAD v2: 9-6428441-A-C
• gnomAD v3: 9-6428441-A-C
• gnomAD v4: 9-6428441-A-C
• MyVariant Identifiers: chr9:g.6428441A>C (hg19) ; chr9:g.6428441A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6428441A>C , CM000671.2:g.6428441A>C	GRCh38
NC_000009.11:g.6428441A>C , CM000671.1:g.6428441A>C	GRCh37
NC_000009.10:g.6418441A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000276893.10:c.385-5473A>C MANE Select	ENSP00000276893.5:n.385-5473A>C
ENST00000276893.9:c.385-5473A>C	ENSP00000276893.5:n.385-5473A>C
ENST00000450508.1:c.-26+7299A>C	ENSP00000399217.1:n.-26+7299A>C
ENST00000461236.1:n.343-5473A>C
ENST00000468435.6:c.385-5473A>C	ENSP00000434182.1:n.385-5473A>C
ENST00000469298.5:n.556-5473A>C
ENST00000481049.5:n.367-5473A>C
NM_152896.2:c.385-5473A>C	NP_690856.1:n.385-5473A>C
NR_046386.1:n.725-5473A>C
XM_011517703.1:c.385-5473A>C	XP_011516005.1:n.385-5473A>C
XM_011517704.1:c.-285-5473A>C	XP_011516006.1:n.-285-5473A>C
XM_011517705.1:c.-26+7299A>C	XP_011516007.1:n.-26+7299A>C
XR_428418.2:n.728-5473A>C
XR_428419.2:n.728-5473A>C
XR_428420.2:n.728-5473A>C
XR_428421.2:n.728-5473A>C
XR_929173.1:n.728-5473A>C
XM_011517704.2:c.-285-5473A>C	XP_011516006.1:n.-285-5473A>C
XM_011517705.2:c.-26+7299A>C	XP_011516007.1:n.-26+7299A>C
XM_017014253.1:c.385-5473A>C	XP_016869742.1:n.385-5473A>C
XM_017014254.1:c.-559-5473A>C	XP_016869743.1:n.-559-5473A>C
XR_001746178.2:n.728-5473A>C
XR_001746179.1:n.728-5473A>C
XR_001746180.2:n.728-5473A>C
XR_001746181.1:n.728-5473A>C
XR_001746182.1:n.728-5473A>C
XR_428418.4:n.728-5473A>C
NM_152896.3:c.385-5473A>C MANE Select	NP_690856.1:n.385-5473A>C
NR_046386.2:n.677-5473A>C