Canonical Allele Identifier: CA10924192
Gene: PDE4B HGNC NCBI

Linked Data

dbSNP Id: rs11208756
gnomAD v2: 1-66269311-T-C
gnomAD v3: 1-65803628-T-C
gnomAD v4: 1-65803628-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.65803628T>C , CM000663.2:g.65803628T>C GRCh38
NC_000001.10:g.66269311T>C , CM000663.1:g.66269311T>C GRCh37
NC_000001.9:g.66041899T>C NCBI36
NG_029038.1:g.16119T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000341517.9:c.-71+10380T>C MANE Select ENSP00000342637.4:n.-71+10380T>C
ENST00000329654.8:c.-71+10998T>C ENSP00000332116.4:n.-71+10998T>C
ENST00000341517.8:c.-71+10380T>C ENSP00000342637.4:n.-71+10380T>C
NM_001037341.1:c.-71+10998T>C NP_001032418.1:n.-71+10998T>C
NM_001297440.1:c.-108+10998T>C NP_001284369.1:n.-108+10998T>C
NM_002600.3:c.-71+10380T>C NP_002591.2:n.-71+10380T>C
NM_002600.4:c.-71+10380T>C MANE Select NP_002591.2:n.-71+10380T>C
NM_001037341.2:c.-71+10998T>C NP_001032418.1:n.-71+10998T>C
NM_001297440.2:c.-108+10998T>C NP_001284369.1:n.-108+10998T>C