Canonical Allele Identifier: CA1953917135

Gene: PDE3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.14752985T= , CM000673.2:g.14752985T=	GRCh38
NC_000011.9:g.14774531T= , CM000673.1:g.14774531T=	GRCh37
NC_000011.8:g.14731107T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282096.9:c.979-18952T= MANE Select	ENSP00000282096.4:n.979-18952T=
ENST00000282096.8:c.979-18952T=	ENSP00000282096.4:n.979-18952T=
ENST00000455098.2:c.979-18952T=	ENSP00000388644.2:n.979-18952T=
ENST00000534317.1:n.795-18952T=
NM_000922.3:c.979-18952T=	NP_000913.2:n.979-18952T=
XM_006718249.2:c.979-18952T=	XP_006718312.1:n.979-18952T=
XM_011520183.1:c.979-18952T=	XP_011518485.1:n.979-18952T=
NM_001363569.1:c.979-18952T=	NP_001350498.1:n.979-18952T=
NM_001363570.1:c.979-18952T=	NP_001350499.1:n.979-18952T=
XM_006718249.3:c.979-18952T=	XP_006718312.1:n.979-18952T=
XM_017017911.2:c.979-18952T=	XP_016873400.1:n.979-18952T=
XM_017017912.1:c.979-18952T=	XP_016873401.1:n.979-18952T=
XR_001747903.2:n.1364-18952T=
NM_000922.4:c.979-18952T= MANE Select	NP_000913.2:n.979-18952T=
NM_001363569.2:c.979-18952T=	NP_001350498.1:n.979-18952T=
NM_001363570.2:c.979-18952T=	NP_001350499.1:n.979-18952T=