Canonical Allele Identifier: CA1142907475

Gene: PDE4B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.65845110T= , CM000663.2:g.65845110T=	GRCh38
NC_000001.10:g.66310793T= , CM000663.1:g.66310793T=	GRCh37
NC_000001.9:g.66083381T=	NCBI36
NG_029038.1:g.57601T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341517.9:c.-71+51862T= MANE Select	ENSP00000342637.4:n.-71+51862T=
ENST00000329654.8:c.-71+52480T=	ENSP00000332116.4:n.-71+52480T=
ENST00000341517.8:c.-71+51862T=	ENSP00000342637.4:n.-71+51862T=
NM_001037341.1:c.-71+52480T=	NP_001032418.1:n.-71+52480T=
NM_001297440.1:c.-108+52480T=	NP_001284369.1:n.-108+52480T=
NM_002600.3:c.-71+51862T=	NP_002591.2:n.-71+51862T=
NM_002600.4:c.-71+51862T= MANE Select	NP_002591.2:n.-71+51862T=
NM_001037341.2:c.-71+52480T=	NP_001032418.1:n.-71+52480T=
NM_001297440.2:c.-108+52480T=	NP_001284369.1:n.-108+52480T=