Canonical Allele Identifier: CA935353442

Gene: PDE3B

Linked Data

• dbSNP Id: rs1857092511
• gnomAD v3: 11-14752922-A-C
• gnomAD v4: 11-14752922-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.14752922A>C , CM000673.2:g.14752922A>C	GRCh38
NC_000011.9:g.14774468A>C , CM000673.1:g.14774468A>C	GRCh37
NC_000011.8:g.14731044A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282096.9:c.979-19015A>C MANE Select	ENSP00000282096.4:n.979-19015A>C
ENST00000282096.8:c.979-19015A>C	ENSP00000282096.4:n.979-19015A>C
ENST00000455098.2:c.979-19015A>C	ENSP00000388644.2:n.979-19015A>C
ENST00000534317.1:n.795-19015A>C
NM_000922.3:c.979-19015A>C	NP_000913.2:n.979-19015A>C
XM_006718249.2:c.979-19015A>C	XP_006718312.1:n.979-19015A>C
XM_011520183.1:c.979-19015A>C	XP_011518485.1:n.979-19015A>C
NM_001363569.1:c.979-19015A>C	NP_001350498.1:n.979-19015A>C
NM_001363570.1:c.979-19015A>C	NP_001350499.1:n.979-19015A>C
XM_006718249.3:c.979-19015A>C	XP_006718312.1:n.979-19015A>C
XM_017017911.2:c.979-19015A>C	XP_016873400.1:n.979-19015A>C
XM_017017912.1:c.979-19015A>C	XP_016873401.1:n.979-19015A>C
XR_001747903.2:n.1364-19015A>C
NM_000922.4:c.979-19015A>C MANE Select	NP_000913.2:n.979-19015A>C
NM_001363569.2:c.979-19015A>C	NP_001350498.1:n.979-19015A>C
NM_001363570.2:c.979-19015A>C	NP_001350499.1:n.979-19015A>C