Canonical Allele Identifier: CA1953917189

Gene: PDE3B

Linked Data

• dbSNP Id: rs1857097707

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.14753095C>G , CM000673.2:g.14753095C>G	GRCh38
NC_000011.9:g.14774641C>G , CM000673.1:g.14774641C>G	GRCh37
NC_000011.8:g.14731217C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000282096.9:c.979-18842C>G MANE Select	ENSP00000282096.4:n.979-18842C>G
ENST00000282096.8:c.979-18842C>G	ENSP00000282096.4:n.979-18842C>G
ENST00000455098.2:c.979-18842C>G	ENSP00000388644.2:n.979-18842C>G
ENST00000534317.1:n.795-18842C>G
NM_000922.3:c.979-18842C>G	NP_000913.2:n.979-18842C>G
XM_006718249.2:c.979-18842C>G	XP_006718312.1:n.979-18842C>G
XM_011520183.1:c.979-18842C>G	XP_011518485.1:n.979-18842C>G
NM_001363569.1:c.979-18842C>G	NP_001350498.1:n.979-18842C>G
NM_001363570.1:c.979-18842C>G	NP_001350499.1:n.979-18842C>G
XM_006718249.3:c.979-18842C>G	XP_006718312.1:n.979-18842C>G
XM_017017911.2:c.979-18842C>G	XP_016873400.1:n.979-18842C>G
XM_017017912.1:c.979-18842C>G	XP_016873401.1:n.979-18842C>G
XR_001747903.2:n.1364-18842C>G
NM_000922.4:c.979-18842C>G MANE Select	NP_000913.2:n.979-18842C>G
NM_001363569.2:c.979-18842C>G	NP_001350498.1:n.979-18842C>G
NM_001363570.2:c.979-18842C>G	NP_001350499.1:n.979-18842C>G