Canonical Allele Identifier: CA379863947

Gene: PDE3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.14644551C>T , CM000673.2:g.14644551C>T	GRCh38
NC_000011.9:g.14666097C>T , CM000673.1:g.14666097C>T	GRCh37
NC_000011.8:g.14622673C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282096.9:c.476C>T MANE Select	ENSP00000282096.4:p.Ala159Val
ENST00000282096.8:c.476C>T	ENSP00000282096.4:p.Ala159Val
ENST00000455098.2:c.476C>T	ENSP00000388644.2:p.Ala159Val
ENST00000534317.1:n.292C>T
NM_000922.3:c.476C>T	NP_000913.2:p.Ala159Val
XM_006718249.2:c.476C>T	XP_006718312.1:p.Ala159Val
XM_011520183.1:c.476C>T	XP_011518485.1:p.Ala159Val
NM_001363569.1:c.476C>T	NP_001350498.1:p.Ala159Val
NM_001363570.1:c.476C>T	NP_001350499.1:p.Ala159Val
XM_006718249.3:c.476C>T	XP_006718312.1:p.Ala159Val
XM_017017911.2:c.476C>T	XP_016873400.1:p.Ala159Val
XM_017017912.1:c.476C>T	XP_016873401.1:p.Ala159Val
XR_001747903.2:n.861C>T
NM_000922.4:c.476C>T MANE Select	NP_000913.2:p.Ala159Val
NM_001363569.2:c.476C>T	NP_001350498.1:p.Ala159Val
NM_001363570.2:c.476C>T	NP_001350499.1:p.Ala159Val