Canonical Allele Identifier: CA1172462335
Gene: PDE4B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.65845090A= , CM000663.2:g.65845090A= GRCh38
NC_000001.10:g.66310773A= , CM000663.1:g.66310773A= GRCh37
NC_000001.9:g.66083361A= NCBI36
NG_029038.1:g.57581A=

Transcript Alleles

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