Canonical Allele Identifier: CA1172569404
Gene: PDE4B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.66092931T= , CM000663.2:g.66092931T= GRCh38
NC_000001.10:g.66558614T= , CM000663.1:g.66558614T= GRCh37
NC_000001.9:g.66331202T= NCBI36
NG_029038.1:g.305422T=

Transcript Alleles

HGVS Amino-acid change
ENST00000341517.9:c.282-154529T= MANE Select ENSP00000342637.4:n.282-154529T=
ENST00000329654.8:c.282-154529T= ENSP00000332116.4:n.282-154529T=
ENST00000341517.8:c.282-154529T= ENSP00000342637.4:n.282-154529T=
ENST00000423207.6:c.236+99789T= ENSP00000392947.2:n.236+99789T=
ENST00000526666.1:n.473+44041T=
ENST00000531358.1:n.528-19839T=
ENST00000532040.1:n.472+29974T=
NM_001037340.2:c.236+99789T= NP_001032417.1:n.236+99789T=
NM_001037341.1:c.282-154529T= NP_001032418.1:n.282-154529T=
NM_001297440.1:c.6-154529T= NP_001284369.1:n.6-154529T=
NM_001297441.1:c.56+52223T= NP_001284370.1:n.56+52223T=
NM_002600.3:c.282-154529T= NP_002591.2:n.282-154529T=
XM_011541565.1:c.17+44041T= XP_011539867.1:n.17+44041T=
XM_011541566.1:c.-287-154529T= XP_011539868.1:n.-287-154529T=
NM_002600.4:c.282-154529T= MANE Select NP_002591.2:n.282-154529T=
NM_001037340.3:c.236+99789T= NP_001032417.1:n.236+99789T=
NM_001037341.2:c.282-154529T= NP_001032418.1:n.282-154529T=
NM_001297440.2:c.6-154529T= NP_001284369.1:n.6-154529T=