Canonical Allele Identifier: CA2696039327
Gene: PDE4B HGNC NCBI

Linked Data

dbSNP Id: rs2101362873

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.65845222C>T , CM000663.2:g.65845222C>T GRCh38
NC_000001.10:g.66310905C>T , CM000663.1:g.66310905C>T GRCh37
NC_000001.9:g.66083493C>T NCBI36
NG_029038.1:g.57713C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000341517.9:c.-71+51974C>T MANE Select ENSP00000342637.4:n.-71+51974C>T
ENST00000329654.8:c.-71+52592C>T ENSP00000332116.4:n.-71+52592C>T
ENST00000341517.8:c.-71+51974C>T ENSP00000342637.4:n.-71+51974C>T
NM_001037341.1:c.-71+52592C>T NP_001032418.1:n.-71+52592C>T
NM_001297440.1:c.-108+52592C>T NP_001284369.1:n.-108+52592C>T
NM_002600.3:c.-71+51974C>T NP_002591.2:n.-71+51974C>T
NM_002600.4:c.-71+51974C>T MANE Select NP_002591.2:n.-71+51974C>T
NM_001037341.2:c.-71+52592C>T NP_001032418.1:n.-71+52592C>T
NM_001297440.2:c.-108+52592C>T NP_001284369.1:n.-108+52592C>T