Canonical Allele Identifier: CA10675057
Gene: PDE4B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs4655595

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.66093076A>G , CM000663.2:g.66093076A>G GRCh38
NC_000001.10:g.66558759A>G , CM000663.1:g.66558759A>G GRCh37
NC_000001.9:g.66331347A>G NCBI36
NG_029038.1:g.305567A>G

Transcript Alleles

HGVS Amino-acid change
NM_001037340.2:c.236+99934A>G VV NP_001032417.1:p.=
NM_001037341.1:c.282-154384A>G VV NP_001032418.1:p.=
NM_001297440.1:c.6-154384A>G VV NP_001284369.1:p.=
NM_001297441.1:c.56+52368A>G VV NP_001284370.1:p.=
NM_002600.3:c.282-154384A>G VV NP_002591.2:p.=
XM_011541565.1:c.17+44186A>G XP_011539867.1:p.=
XM_011541566.1:c.-287-154384A>G XP_011539868.1:p.=
NM_002600.4:c.282-154384A>G VV MANE Preferred NP_002591.2:p.=
ENST00000329654.8:c.282-154384A>G ENSP00000332116.4:p.=
ENST00000341517.8:c.282-154384A>G ENSP00000342637.4:p.=
ENST00000423207.6:c.236+99934A>G ENSP00000392947.2:p.=
ENST00000526666.1:n.473+44186A>G
ENST00000531358.1:n.528-19694A>G
ENST00000532040.1:n.472+30119A>G