Canonical Allele Identifier: CA1002648993
Gene: PDE4B HGNC NCBI

Linked Data

dbSNP Id: rs1646254604
gnomAD v3: 1-65845159-A-G
gnomAD v4: 1-65845159-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.65845159A>G , CM000663.2:g.65845159A>G GRCh38
NC_000001.10:g.66310842A>G , CM000663.1:g.66310842A>G GRCh37
NC_000001.9:g.66083430A>G NCBI36
NG_029038.1:g.57650A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000341517.9:c.-71+51911A>G MANE Select ENSP00000342637.4:n.-71+51911A>G
ENST00000329654.8:c.-71+52529A>G ENSP00000332116.4:n.-71+52529A>G
ENST00000341517.8:c.-71+51911A>G ENSP00000342637.4:n.-71+51911A>G
NM_001037341.1:c.-71+52529A>G NP_001032418.1:n.-71+52529A>G
NM_001297440.1:c.-108+52529A>G NP_001284369.1:n.-108+52529A>G
NM_002600.3:c.-71+51911A>G NP_002591.2:n.-71+51911A>G
NM_002600.4:c.-71+51911A>G MANE Select NP_002591.2:n.-71+51911A>G
NM_001037341.2:c.-71+52529A>G NP_001032418.1:n.-71+52529A>G
NM_001297440.2:c.-108+52529A>G NP_001284369.1:n.-108+52529A>G