Canonical Allele Identifier: CA1172462502
Gene: PDE4B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.65845321A= , CM000663.2:g.65845321A= GRCh38
NC_000001.10:g.66311004A= , CM000663.1:g.66311004A= GRCh37
NC_000001.9:g.66083592A= NCBI36
NG_029038.1:g.57812A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000341517.9:c.-71+52073A= MANE Select ENSP00000342637.4:n.-71+52073A=
ENST00000329654.8:c.-71+52691A= ENSP00000332116.4:n.-71+52691A=
ENST00000341517.8:c.-71+52073A= ENSP00000342637.4:n.-71+52073A=
NM_001037341.1:c.-71+52691A= NP_001032418.1:n.-71+52691A=
NM_001297440.1:c.-108+52691A= NP_001284369.1:n.-108+52691A=
NM_002600.3:c.-71+52073A= NP_002591.2:n.-71+52073A=
NM_002600.4:c.-71+52073A= MANE Select NP_002591.2:n.-71+52073A=
NM_001037341.2:c.-71+52691A= NP_001032418.1:n.-71+52691A=
NM_001297440.2:c.-108+52691A= NP_001284369.1:n.-108+52691A=
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