Canonical Allele Identifier: CA1002648985
Gene: PDE4B HGNC NCBI

Linked Data

dbSNP Id: rs1646254325
gnomAD v3: 1-65845143-G-A
gnomAD v4: 1-65845143-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.65845143G>A , CM000663.2:g.65845143G>A GRCh38
NC_000001.10:g.66310826G>A , CM000663.1:g.66310826G>A GRCh37
NC_000001.9:g.66083414G>A NCBI36
NG_029038.1:g.57634G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000341517.9:c.-71+51895G>A MANE Select ENSP00000342637.4:n.-71+51895G>A
ENST00000329654.8:c.-71+52513G>A ENSP00000332116.4:n.-71+52513G>A
ENST00000341517.8:c.-71+51895G>A ENSP00000342637.4:n.-71+51895G>A
NM_001037341.1:c.-71+52513G>A NP_001032418.1:n.-71+52513G>A
NM_001297440.1:c.-108+52513G>A NP_001284369.1:n.-108+52513G>A
NM_002600.3:c.-71+51895G>A NP_002591.2:n.-71+51895G>A
NM_002600.4:c.-71+51895G>A MANE Select NP_002591.2:n.-71+51895G>A
NM_001037341.2:c.-71+52513G>A NP_001032418.1:n.-71+52513G>A
NM_001297440.2:c.-108+52513G>A NP_001284369.1:n.-108+52513G>A
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