Canonical Allele Identifier: CA15706667
Gene: PDE3B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14762564G>C , CM000673.2:g.14762564G>C GRCh38
NC_000011.9:g.14784110G>C , CM000673.1:g.14784110G>C GRCh37
NC_000011.8:g.14740686G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000282096.9:c.979-9373G>C MANE Select ENSP00000282096.4:n.979-9373G>C
ENST00000282096.8:c.979-9373G>C ENSP00000282096.4:n.979-9373G>C
ENST00000455098.2:c.979-9373G>C ENSP00000388644.2:n.979-9373G>C
ENST00000534317.1:n.795-9373G>C
NM_000922.3:c.979-9373G>C NP_000913.2:n.979-9373G>C
XM_006718249.2:c.979-9373G>C XP_006718312.1:n.979-9373G>C
XM_011520183.1:c.979-9373G>C XP_011518485.1:n.979-9373G>C
NM_001363569.1:c.979-9373G>C NP_001350498.1:n.979-9373G>C
NM_001363570.1:c.979-9373G>C NP_001350499.1:n.979-9373G>C
XM_006718249.3:c.979-9373G>C XP_006718312.1:n.979-9373G>C
XM_017017911.2:c.979-9373G>C XP_016873400.1:n.979-9373G>C
XM_017017912.1:c.979-9373G>C XP_016873401.1:n.979-9373G>C
XR_001747903.2:n.1364-9373G>C
NM_000922.4:c.979-9373G>C MANE Select NP_000913.2:n.979-9373G>C
NM_001363569.2:c.979-9373G>C NP_001350498.1:n.979-9373G>C
NM_001363570.2:c.979-9373G>C NP_001350499.1:n.979-9373G>C
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