Canonical Allele Identifier: CA1172569362

Gene: PDE4B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.66092838G= , CM000663.2:g.66092838G=	GRCh38
NC_000001.10:g.66558521G= , CM000663.1:g.66558521G=	GRCh37
NC_000001.9:g.66331109G=	NCBI36
NG_029038.1:g.305329G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341517.9:c.282-154622G= MANE Select	ENSP00000342637.4:n.282-154622G=
ENST00000329654.8:c.282-154622G=	ENSP00000332116.4:n.282-154622G=
ENST00000341517.8:c.282-154622G=	ENSP00000342637.4:n.282-154622G=
ENST00000423207.6:c.236+99696G=	ENSP00000392947.2:n.236+99696G=
ENST00000526666.1:n.473+43948G=
ENST00000531358.1:n.528-19932G=
ENST00000532040.1:n.472+29881G=
NM_001037340.2:c.236+99696G=	NP_001032417.1:n.236+99696G=
NM_001037341.1:c.282-154622G=	NP_001032418.1:n.282-154622G=
NM_001297440.1:c.6-154622G=	NP_001284369.1:n.6-154622G=
NM_001297441.1:c.56+52130G=	NP_001284370.1:n.56+52130G=
NM_002600.3:c.282-154622G=	NP_002591.2:n.282-154622G=
XM_011541565.1:c.17+43948G=	XP_011539867.1:n.17+43948G=
XM_011541566.1:c.-287-154622G=	XP_011539868.1:n.-287-154622G=
NM_002600.4:c.282-154622G= MANE Select	NP_002591.2:n.282-154622G=
NM_001037340.3:c.236+99696G=	NP_001032417.1:n.236+99696G=
NM_001037341.2:c.282-154622G=	NP_001032418.1:n.282-154622G=
NM_001297440.2:c.6-154622G=	NP_001284369.1:n.6-154622G=