Canonical Allele Identifier: CA224435613
Gene: PDE2A HGNC NCBI
PDE2A-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1023372470
MyVariant Identifiers: chr11:g.72662545G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72662545G>C , CM000673.2:g.72662545G>C GRCh38
NC_000011.9:g.72373589G>C , CM000673.1:g.72373589G>C GRCh37
NC_000011.8:g.72051237G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000334456.10:c.71+11592C>G (PDE2A) MANE Select ENSP00000334910.5:n.71+11592C>G
ENST00000334456.9:c.71+11592C>G (PDE2A) ENSP00000334910.5:n.71+11592C>G
ENST00000418754.6:c.71+11592C>G (PDE2A) ENSP00000410310.2:n.71+11592C>G
ENST00000535701.1:c.71+11592C>G (PDE2A) ENSP00000439302.1:n.71+11592C>G
ENST00000540345.5:c.44+5753C>G (PDE2A) ENSP00000446399.1:n.44+5753C>G
ENST00000540380.5:n.455+11592C>G (PDE2A)
ENST00000542969.2:c.-55+11592C>G (PDE2A) ENSP00000443232.1:n.-55+11592C>G
ENST00000546038.1:c.*80+5753C>G (PDE2A) ENSP00000438295.1:n.*80+5753C>G
NM_001146209.2:c.44+5753C>G (PDE2A) NP_001139681.1:n.44+5753C>G
NM_002599.4:c.71+11592C>G (PDE2A) NP_002590.1:n.71+11592C>G
XR_950288.1:n.508+1700G>C (PDE2A-AS1)
XR_001748293.1:n.750+1700G>C (PDE2A-AS1)
XR_950288.3:n.726+1700G>C (PDE2A-AS1)
NM_002599.5:c.71+11592C>G (PDE2A) MANE Select NP_002590.1:n.71+11592C>G
NM_001146209.3:c.44+5753C>G (PDE2A) NP_001139681.1:n.44+5753C>G