Canonical Allele Identifier: CA1172462426
Gene: PDE4B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.65845213G= , CM000663.2:g.65845213G= GRCh38
NC_000001.10:g.66310896G= , CM000663.1:g.66310896G= GRCh37
NC_000001.9:g.66083484G= NCBI36
NG_029038.1:g.57704G=

Transcript Alleles

HGVS Amino-acid change
ENST00000341517.9:c.-71+51965G= MANE Select ENSP00000342637.4:n.-71+51965G=
ENST00000329654.8:c.-71+52583G= ENSP00000332116.4:n.-71+52583G=
ENST00000341517.8:c.-71+51965G= ENSP00000342637.4:n.-71+51965G=
NM_001037341.1:c.-71+52583G= NP_001032418.1:n.-71+52583G=
NM_001297440.1:c.-108+52583G= NP_001284369.1:n.-108+52583G=
NM_002600.3:c.-71+51965G= NP_002591.2:n.-71+51965G=
NM_002600.4:c.-71+51965G= MANE Select NP_002591.2:n.-71+51965G=
NM_001037341.2:c.-71+52583G= NP_001032418.1:n.-71+52583G=
NM_001297440.2:c.-108+52583G= NP_001284369.1:n.-108+52583G=