Canonical Allele Identifier: CA1172569407
Gene: PDE4B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.66092937G= , CM000663.2:g.66092937G= GRCh38
NC_000001.10:g.66558620G= , CM000663.1:g.66558620G= GRCh37
NC_000001.9:g.66331208G= NCBI36
NG_029038.1:g.305428G=

Transcript Alleles

HGVS Amino-acid change
ENST00000341517.9:c.282-154523G= MANE Select ENSP00000342637.4:n.282-154523G=
ENST00000329654.8:c.282-154523G= ENSP00000332116.4:n.282-154523G=
ENST00000341517.8:c.282-154523G= ENSP00000342637.4:n.282-154523G=
ENST00000423207.6:c.236+99795G= ENSP00000392947.2:n.236+99795G=
ENST00000526666.1:n.473+44047G=
ENST00000531358.1:n.528-19833G=
ENST00000532040.1:n.472+29980G=
NM_001037340.2:c.236+99795G= NP_001032417.1:n.236+99795G=
NM_001037341.1:c.282-154523G= NP_001032418.1:n.282-154523G=
NM_001297440.1:c.6-154523G= NP_001284369.1:n.6-154523G=
NM_001297441.1:c.56+52229G= NP_001284370.1:n.56+52229G=
NM_002600.3:c.282-154523G= NP_002591.2:n.282-154523G=
XM_011541565.1:c.17+44047G= XP_011539867.1:n.17+44047G=
XM_011541566.1:c.-287-154523G= XP_011539868.1:n.-287-154523G=
NM_002600.4:c.282-154523G= MANE Select NP_002591.2:n.282-154523G=
NM_001037340.3:c.236+99795G= NP_001032417.1:n.236+99795G=
NM_001037341.2:c.282-154523G= NP_001032418.1:n.282-154523G=
NM_001297440.2:c.6-154523G= NP_001284369.1:n.6-154523G=