Canonical Allele Identifier: CA673975473

Gene: PDE3B

Linked Data

• dbSNP Id: rs1239871732
• gnomAD v3: 11-14753131-T-C
• gnomAD v4: 11-14753131-T-C
• MyVariant Identifiers: chr11:g.14774677T>C (hg19) ; chr11:g.14753131T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.14753131T>C , CM000673.2:g.14753131T>C	GRCh38
NC_000011.9:g.14774677T>C , CM000673.1:g.14774677T>C	GRCh37
NC_000011.8:g.14731253T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000282096.9:c.979-18806T>C MANE Select	ENSP00000282096.4:n.979-18806T>C
ENST00000282096.8:c.979-18806T>C	ENSP00000282096.4:n.979-18806T>C
ENST00000455098.2:c.979-18806T>C	ENSP00000388644.2:n.979-18806T>C
ENST00000534317.1:n.795-18806T>C
NM_000922.3:c.979-18806T>C	NP_000913.2:n.979-18806T>C
XM_006718249.2:c.979-18806T>C	XP_006718312.1:n.979-18806T>C
XM_011520183.1:c.979-18806T>C	XP_011518485.1:n.979-18806T>C
NM_001363569.1:c.979-18806T>C	NP_001350498.1:n.979-18806T>C
NM_001363570.1:c.979-18806T>C	NP_001350499.1:n.979-18806T>C
XM_006718249.3:c.979-18806T>C	XP_006718312.1:n.979-18806T>C
XM_017017911.2:c.979-18806T>C	XP_016873400.1:n.979-18806T>C
XM_017017912.1:c.979-18806T>C	XP_016873401.1:n.979-18806T>C
XR_001747903.2:n.1364-18806T>C
NM_000922.4:c.979-18806T>C MANE Select	NP_000913.2:n.979-18806T>C
NM_001363569.2:c.979-18806T>C	NP_001350498.1:n.979-18806T>C
NM_001363570.2:c.979-18806T>C	NP_001350499.1:n.979-18806T>C