Canonical Allele Identifier: CA1172569414
Gene: PDE4B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.66092959A= , CM000663.2:g.66092959A= GRCh38
NC_000001.10:g.66558642A= , CM000663.1:g.66558642A= GRCh37
NC_000001.9:g.66331230A= NCBI36
NG_029038.1:g.305450A=

Transcript Alleles

HGVS Amino-acid change
ENST00000341517.9:c.282-154501A= MANE Select ENSP00000342637.4:n.282-154501A=
ENST00000329654.8:c.282-154501A= ENSP00000332116.4:n.282-154501A=
ENST00000341517.8:c.282-154501A= ENSP00000342637.4:n.282-154501A=
ENST00000423207.6:c.236+99817A= ENSP00000392947.2:n.236+99817A=
ENST00000526666.1:n.473+44069A=
ENST00000531358.1:n.528-19811A=
ENST00000532040.1:n.472+30002A=
NM_001037340.2:c.236+99817A= NP_001032417.1:n.236+99817A=
NM_001037341.1:c.282-154501A= NP_001032418.1:n.282-154501A=
NM_001297440.1:c.6-154501A= NP_001284369.1:n.6-154501A=
NM_001297441.1:c.56+52251A= NP_001284370.1:n.56+52251A=
NM_002600.3:c.282-154501A= NP_002591.2:n.282-154501A=
XM_011541565.1:c.17+44069A= XP_011539867.1:n.17+44069A=
XM_011541566.1:c.-287-154501A= XP_011539868.1:n.-287-154501A=
NM_002600.4:c.282-154501A= MANE Select NP_002591.2:n.282-154501A=
NM_001037340.3:c.236+99817A= NP_001032417.1:n.236+99817A=
NM_001037341.2:c.282-154501A= NP_001032418.1:n.282-154501A=
NM_001297440.2:c.6-154501A= NP_001284369.1:n.6-154501A=