Canonical Allele Identifier: CA10772887
Gene: PDE4B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.66296783T>C , CM000663.2:g.66296783T>C GRCh38
NC_000001.10:g.66762466T>C , CM000663.1:g.66762466T>C GRCh37
NC_000001.9:g.66535054T>C NCBI36
NG_029038.1:g.509274T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000341517.9:c.634+30696T>C MANE Select ENSP00000342637.4:n.634+30696T>C
ENST00000329654.8:c.634+30696T>C ENSP00000332116.4:n.634+30696T>C
ENST00000341517.8:c.634+30696T>C ENSP00000342637.4:n.634+30696T>C
ENST00000412480.6:c.358+30696T>C ENSP00000397548.2:n.358+30696T>C
ENST00000423207.6:c.589+30696T>C ENSP00000392947.2:n.589+30696T>C
NM_001037340.2:c.589+30696T>C NP_001032417.1:n.589+30696T>C
NM_001037341.1:c.634+30696T>C NP_001032418.1:n.634+30696T>C
NM_001297440.1:c.358+30696T>C NP_001284369.1:n.358+30696T>C
NM_001297441.1:c.409+30696T>C NP_001284370.1:n.409+30696T>C
NM_002600.3:c.634+30696T>C NP_002591.2:n.634+30696T>C
XM_011541565.1:c.370+30696T>C XP_011539867.1:n.370+30696T>C
XM_011541566.1:c.17-35725T>C XP_011539868.1:n.17-35725T>C
XM_017001445.1:c.217+30696T>C XP_016856934.1:n.217+30696T>C
NM_002600.4:c.634+30696T>C MANE Select NP_002591.2:n.634+30696T>C
NM_001037340.3:c.589+30696T>C NP_001032417.1:n.589+30696T>C
NM_001037341.2:c.634+30696T>C NP_001032418.1:n.634+30696T>C
NM_001297440.2:c.358+30696T>C NP_001284369.1:n.358+30696T>C
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