Canonical Allele Identifier: CA1140248228

Gene: PDE4B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.65803628T= , CM000663.2:g.65803628T=	GRCh38
NC_000001.10:g.66269311T= , CM000663.1:g.66269311T=	GRCh37
NC_000001.9:g.66041899T=	NCBI36
NG_029038.1:g.16119T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341517.9:c.-71+10380T= MANE Select	ENSP00000342637.4:n.-71+10380T=
ENST00000329654.8:c.-71+10998T=	ENSP00000332116.4:n.-71+10998T=
ENST00000341517.8:c.-71+10380T=	ENSP00000342637.4:n.-71+10380T=
NM_001037341.1:c.-71+10998T=	NP_001032418.1:n.-71+10998T=
NM_001297440.1:c.-108+10998T=	NP_001284369.1:n.-108+10998T=
NM_002600.3:c.-71+10380T=	NP_002591.2:n.-71+10380T=
NM_002600.4:c.-71+10380T= MANE Select	NP_002591.2:n.-71+10380T=
NM_001037341.2:c.-71+10998T=	NP_001032418.1:n.-71+10998T=
NM_001297440.2:c.-108+10998T=	NP_001284369.1:n.-108+10998T=