Canonical Allele Identifier: CA738027381

Gene: PDE4B

Linked Data

• dbSNP Id: rs1447428120
• gnomAD v3: 1-66092828-G-T
• gnomAD v4: 1-66092828-G-T
• MyVariant Identifiers: chr1:g.66558511G>T (hg19) ; chr1:g.66092828G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.66092828G>T , CM000663.2:g.66092828G>T	GRCh38
NC_000001.10:g.66558511G>T , CM000663.1:g.66558511G>T	GRCh37
NC_000001.9:g.66331099G>T	NCBI36
NG_029038.1:g.305319G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341517.9:c.282-154632G>T MANE Select	ENSP00000342637.4:n.282-154632G>T
ENST00000329654.8:c.282-154632G>T	ENSP00000332116.4:n.282-154632G>T
ENST00000341517.8:c.282-154632G>T	ENSP00000342637.4:n.282-154632G>T
ENST00000423207.6:c.236+99686G>T	ENSP00000392947.2:n.236+99686G>T
ENST00000526666.1:n.473+43938G>T
ENST00000531358.1:n.528-19942G>T
ENST00000532040.1:n.472+29871G>T
NM_001037340.2:c.236+99686G>T	NP_001032417.1:n.236+99686G>T
NM_001037341.1:c.282-154632G>T	NP_001032418.1:n.282-154632G>T
NM_001297440.1:c.6-154632G>T	NP_001284369.1:n.6-154632G>T
NM_001297441.1:c.56+52120G>T	NP_001284370.1:n.56+52120G>T
NM_002600.3:c.282-154632G>T	NP_002591.2:n.282-154632G>T
XM_011541565.1:c.17+43938G>T	XP_011539867.1:n.17+43938G>T
XM_011541566.1:c.-287-154632G>T	XP_011539868.1:n.-287-154632G>T
NM_002600.4:c.282-154632G>T MANE Select	NP_002591.2:n.282-154632G>T
NM_001037340.3:c.236+99686G>T	NP_001032417.1:n.236+99686G>T
NM_001037341.2:c.282-154632G>T	NP_001032418.1:n.282-154632G>T
NM_001297440.2:c.6-154632G>T	NP_001284369.1:n.6-154632G>T