Canonical Allele Identifier: CA738007465
Gene: PDE4B HGNC NCBI

Linked Data

dbSNP Id: rs1435909508

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.65845090_65845091del , CM000663.2:g.65845090_65845091del GRCh38
NC_000001.10:g.66310773_66310774del , CM000663.1:g.66310773_66310774del GRCh37
NC_000001.9:g.66083361_66083362del NCBI36
NG_029038.1:g.57581_57582del

Transcript Alleles

HGVS Amino-acid change
ENST00000341517.9:c.-71+51842_-71+51843del MANE Select ENSP00000342637.4:n.-71+51842_-71+51843de...
ENST00000329654.8:c.-71+52460_-71+52461del ENSP00000332116.4:n.-71+52460_-71+52461de...
ENST00000341517.8:c.-71+51842_-71+51843del ENSP00000342637.4:n.-71+51842_-71+51843de...
NM_001037341.1:c.-71+52460_-71+52461del NP_001032418.1:n.-71+52460_-71+52461del
NM_001297440.1:c.-108+52460_-108+52461del NP_001284369.1:n.-108+52460_-108+52461del...
NM_002600.3:c.-71+51842_-71+51843del NP_002591.2:n.-71+51842_-71+51843del
NM_002600.4:c.-71+51842_-71+51843del MANE Select NP_002591.2:n.-71+51842_-71+51843del
NM_001037341.2:c.-71+52460_-71+52461del NP_001032418.1:n.-71+52460_-71+52461del
NM_001297440.2:c.-108+52460_-108+52461del NP_001284369.1:n.-108+52460_-108+52461del...