Canonical Allele Identifier: CA1140019886

Gene: PDE4B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.65813442A= , CM000663.2:g.65813442A=	GRCh38
NC_000001.10:g.66279125A= , CM000663.1:g.66279125A=	GRCh37
NC_000001.9:g.66051713A=	NCBI36
NG_029038.1:g.25933A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341517.9:c.-71+20194A= MANE Select	ENSP00000342637.4:n.-71+20194A=
ENST00000329654.8:c.-71+20812A=	ENSP00000332116.4:n.-71+20812A=
ENST00000341517.8:c.-71+20194A=	ENSP00000342637.4:n.-71+20194A=
NM_001037341.1:c.-71+20812A=	NP_001032418.1:n.-71+20812A=
NM_001297440.1:c.-108+20812A=	NP_001284369.1:n.-108+20812A=
NM_002600.3:c.-71+20194A=	NP_002591.2:n.-71+20194A=
NM_002600.4:c.-71+20194A= MANE Select	NP_002591.2:n.-71+20194A=
NM_001037341.2:c.-71+20812A=	NP_001032418.1:n.-71+20812A=
NM_001297440.2:c.-108+20812A=	NP_001284369.1:n.-108+20812A=