Canonical Allele Identifier: CA1172462432
Gene: PDE4B HGNC NCBI

Linked Data

dbSNP Id: rs1646255314
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.65845216G>A , CM000663.2:g.65845216G>A GRCh38
NC_000001.10:g.66310899G>A , CM000663.1:g.66310899G>A GRCh37
NC_000001.9:g.66083487G>A NCBI36
NG_029038.1:g.57707G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000341517.9:c.-71+51968G>A MANE Select ENSP00000342637.4:n.-71+51968G>A
ENST00000329654.8:c.-71+52586G>A ENSP00000332116.4:n.-71+52586G>A
ENST00000341517.8:c.-71+51968G>A ENSP00000342637.4:n.-71+51968G>A
NM_001037341.1:c.-71+52586G>A NP_001032418.1:n.-71+52586G>A
NM_001297440.1:c.-108+52586G>A NP_001284369.1:n.-108+52586G>A
NM_002600.3:c.-71+51968G>A NP_002591.2:n.-71+51968G>A
NM_002600.4:c.-71+51968G>A MANE Select NP_002591.2:n.-71+51968G>A
NM_001037341.2:c.-71+52586G>A NP_001032418.1:n.-71+52586G>A
NM_001297440.2:c.-108+52586G>A NP_001284369.1:n.-108+52586G>A
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