Canonical Allele Identifier: CA1172569402

Gene: PDE4B

Linked Data

• dbSNP Id: rs1645051806

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.66092926G>A , CM000663.2:g.66092926G>A	GRCh38
NC_000001.10:g.66558609G>A , CM000663.1:g.66558609G>A	GRCh37
NC_000001.9:g.66331197G>A	NCBI36
NG_029038.1:g.305417G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000341517.9:c.282-154534G>A MANE Select	ENSP00000342637.4:n.282-154534G>A
ENST00000329654.8:c.282-154534G>A	ENSP00000332116.4:n.282-154534G>A
ENST00000341517.8:c.282-154534G>A	ENSP00000342637.4:n.282-154534G>A
ENST00000423207.6:c.236+99784G>A	ENSP00000392947.2:n.236+99784G>A
ENST00000526666.1:n.473+44036G>A
ENST00000531358.1:n.528-19844G>A
ENST00000532040.1:n.472+29969G>A
NM_001037340.2:c.236+99784G>A	NP_001032417.1:n.236+99784G>A
NM_001037341.1:c.282-154534G>A	NP_001032418.1:n.282-154534G>A
NM_001297440.1:c.6-154534G>A	NP_001284369.1:n.6-154534G>A
NM_001297441.1:c.56+52218G>A	NP_001284370.1:n.56+52218G>A
NM_002600.3:c.282-154534G>A	NP_002591.2:n.282-154534G>A
XM_011541565.1:c.17+44036G>A	XP_011539867.1:n.17+44036G>A
XM_011541566.1:c.-287-154534G>A	XP_011539868.1:n.-287-154534G>A
NM_002600.4:c.282-154534G>A MANE Select	NP_002591.2:n.282-154534G>A
NM_001037340.3:c.236+99784G>A	NP_001032417.1:n.236+99784G>A
NM_001037341.2:c.282-154534G>A	NP_001032418.1:n.282-154534G>A
NM_001297440.2:c.6-154534G>A	NP_001284369.1:n.6-154534G>A