Canonical Allele Identifier: CA10840163
Gene: PDE4B HGNC NCBI

Linked Data

dbSNP Id: rs4384209
gnomAD v2: 1-66279125-A-G
gnomAD v3: 1-65813442-A-G
gnomAD v4: 1-65813442-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.65813442A>G , CM000663.2:g.65813442A>G GRCh38
NC_000001.10:g.66279125A>G , CM000663.1:g.66279125A>G GRCh37
NC_000001.9:g.66051713A>G NCBI36
NG_029038.1:g.25933A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000341517.9:c.-71+20194A>G MANE Select ENSP00000342637.4:n.-71+20194A>G
ENST00000329654.8:c.-71+20812A>G ENSP00000332116.4:n.-71+20812A>G
ENST00000341517.8:c.-71+20194A>G ENSP00000342637.4:n.-71+20194A>G
NM_001037341.1:c.-71+20812A>G NP_001032418.1:n.-71+20812A>G
NM_001297440.1:c.-108+20812A>G NP_001284369.1:n.-108+20812A>G
NM_002600.3:c.-71+20194A>G NP_002591.2:n.-71+20194A>G
NM_002600.4:c.-71+20194A>G MANE Select NP_002591.2:n.-71+20194A>G
NM_001037341.2:c.-71+20812A>G NP_001032418.1:n.-71+20812A>G
NM_001297440.2:c.-108+20812A>G NP_001284369.1:n.-108+20812A>G