Canonical Allele Identifier: CA218207381

Gene: PDE3B

Linked Data

• dbSNP Id: rs764549733
• gnomAD v3: 11-14752770-G-GTAC
• gnomAD v4: 11-14752770-G-GTAC
• MyVariant Identifiers: chr11:g.14774316_14774317insTAC (hg19) ; chr11:g.14752770_14752771insTAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.14752771_14752773dup , CM000673.2:g.14752771_14752773dup	GRCh38
NC_000011.9:g.14774317_14774319dup , CM000673.1:g.14774317_14774319dup	GRCh37
NC_000011.8:g.14730893_14730895dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282096.9:c.979-19166_979-19164dup MANE Select	ENSP00000282096.4:n.979-19166_979-19164dup
ENST00000282096.8:c.979-19166_979-19164dup	ENSP00000282096.4:n.979-19166_979-19164dup
ENST00000455098.2:c.979-19166_979-19164dup	ENSP00000388644.2:n.979-19166_979-19164dup
ENST00000534317.1:n.795-19166_795-19164dup
NM_000922.3:c.979-19166_979-19164dup	NP_000913.2:n.979-19166_979-19164dup
XM_006718249.2:c.979-19166_979-19164dup	XP_006718312.1:n.979-19166_979-19164dup
XM_011520183.1:c.979-19166_979-19164dup	XP_011518485.1:n.979-19166_979-19164dup
NM_001363569.1:c.979-19166_979-19164dup	NP_001350498.1:n.979-19166_979-19164dup
NM_001363570.1:c.979-19166_979-19164dup	NP_001350499.1:n.979-19166_979-19164dup
XM_006718249.3:c.979-19166_979-19164dup	XP_006718312.1:n.979-19166_979-19164dup
XM_017017911.2:c.979-19166_979-19164dup	XP_016873400.1:n.979-19166_979-19164dup
XM_017017912.1:c.979-19166_979-19164dup	XP_016873401.1:n.979-19166_979-19164dup
XR_001747903.2:n.1364-19166_1364-19164dup
NM_000922.4:c.979-19166_979-19164dup MANE Select	NP_000913.2:n.979-19166_979-19164dup
NM_001363569.2:c.979-19166_979-19164dup	NP_001350498.1:n.979-19166_979-19164dup
NM_001363570.2:c.979-19166_979-19164dup	NP_001350499.1:n.979-19166_979-19164dup