Canonical Allele Identifier: CA218207412

Gene: PDE3B

Linked Data

• dbSNP Id: rs749171334
• MyVariant Identifiers: chr11:g.14774605A>T (hg19) ; chr11:g.14753059A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.14753059A>T , CM000673.2:g.14753059A>T	GRCh38
NC_000011.9:g.14774605A>T , CM000673.1:g.14774605A>T	GRCh37
NC_000011.8:g.14731181A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000282096.9:c.979-18878A>T MANE Select	ENSP00000282096.4:n.979-18878A>T
ENST00000282096.8:c.979-18878A>T	ENSP00000282096.4:n.979-18878A>T
ENST00000455098.2:c.979-18878A>T	ENSP00000388644.2:n.979-18878A>T
ENST00000534317.1:n.795-18878A>T
NM_000922.3:c.979-18878A>T	NP_000913.2:n.979-18878A>T
XM_006718249.2:c.979-18878A>T	XP_006718312.1:n.979-18878A>T
XM_011520183.1:c.979-18878A>T	XP_011518485.1:n.979-18878A>T
NM_001363569.1:c.979-18878A>T	NP_001350498.1:n.979-18878A>T
NM_001363570.1:c.979-18878A>T	NP_001350499.1:n.979-18878A>T
XM_006718249.3:c.979-18878A>T	XP_006718312.1:n.979-18878A>T
XM_017017911.2:c.979-18878A>T	XP_016873400.1:n.979-18878A>T
XM_017017912.1:c.979-18878A>T	XP_016873401.1:n.979-18878A>T
XR_001747903.2:n.1364-18878A>T
NM_000922.4:c.979-18878A>T MANE Select	NP_000913.2:n.979-18878A>T
NM_001363569.2:c.979-18878A>T	NP_001350498.1:n.979-18878A>T
NM_001363570.2:c.979-18878A>T	NP_001350499.1:n.979-18878A>T