Canonical Allele Identifier: CA1172462322

Gene: PDE4B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.65845053G= , CM000663.2:g.65845053G=	GRCh38
NC_000001.10:g.66310736G= , CM000663.1:g.66310736G=	GRCh37
NC_000001.9:g.66083324G=	NCBI36
NG_029038.1:g.57544G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341517.9:c.-71+51805G= MANE Select	ENSP00000342637.4:n.-71+51805G=
ENST00000329654.8:c.-71+52423G=	ENSP00000332116.4:n.-71+52423G=
ENST00000341517.8:c.-71+51805G=	ENSP00000342637.4:n.-71+51805G=
NM_001037341.1:c.-71+52423G=	NP_001032418.1:n.-71+52423G=
NM_001297440.1:c.-108+52423G=	NP_001284369.1:n.-108+52423G=
NM_002600.3:c.-71+51805G=	NP_002591.2:n.-71+51805G=
NM_002600.4:c.-71+51805G= MANE Select	NP_002591.2:n.-71+51805G=
NM_001037341.2:c.-71+52423G=	NP_001032418.1:n.-71+52423G=
NM_001297440.2:c.-108+52423G=	NP_001284369.1:n.-108+52423G=