Canonical Allele Identifier: CA13464069
Gene: PDE2A HGNC NCBI
PDE2A-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs3781913
gnomAD v2: 11-72373496-T-G
gnomAD v3: 11-72662452-T-G
gnomAD v4: 11-72662452-T-G
MyVariant Identifiers: chr11:g.72373496T>G (hg19) chr11:g.72662452T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72662452T>G , CM000673.2:g.72662452T>G GRCh38
NC_000011.9:g.72373496T>G , CM000673.1:g.72373496T>G GRCh37
NC_000011.8:g.72051144T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000334456.10:c.71+11685A>C (PDE2A) MANE Select ENSP00000334910.5:n.71+11685A>C
ENST00000334456.9:c.71+11685A>C (PDE2A) ENSP00000334910.5:n.71+11685A>C
ENST00000418754.6:c.71+11685A>C (PDE2A) ENSP00000410310.2:n.71+11685A>C
ENST00000535701.1:c.71+11685A>C (PDE2A) ENSP00000439302.1:n.71+11685A>C
ENST00000540345.5:c.44+5846A>C (PDE2A) ENSP00000446399.1:n.44+5846A>C
ENST00000540380.5:n.455+11685A>C (PDE2A)
ENST00000542969.2:c.-55+11685A>C (PDE2A) ENSP00000443232.1:n.-55+11685A>C
ENST00000546038.1:c.*80+5846A>C (PDE2A) ENSP00000438295.1:n.*80+5846A>C
NM_001146209.2:c.44+5846A>C (PDE2A) NP_001139681.1:n.44+5846A>C
NM_002599.4:c.71+11685A>C (PDE2A) NP_002590.1:n.71+11685A>C
XR_950288.1:n.508+1607T>G (PDE2A-AS1)
XR_001748293.1:n.750+1607T>G (PDE2A-AS1)
XR_950288.3:n.726+1607T>G (PDE2A-AS1)
NM_002599.5:c.71+11685A>C (PDE2A) MANE Select NP_002590.1:n.71+11685A>C
NM_001146209.3:c.44+5846A>C (PDE2A) NP_001139681.1:n.44+5846A>C
Search 100 bp 5'
Search 100 bp 3'