Canonical Allele Identifier: CA1002679946

Gene: PDE4B

Linked Data

• dbSNP Id: rs1321172
• gnomAD v3: 1-66265030-C-T
• gnomAD v4: 1-66265030-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.66265030C>T , CM000663.2:g.66265030C>T	GRCh38
NC_000001.10:g.66730713C>T , CM000663.1:g.66730713C>T	GRCh37
NC_000001.9:g.66503301C>T	NCBI36
NG_029038.1:g.477521C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000341517.9:c.585-1008C>T MANE Select	ENSP00000342637.4:n.585-1008C>T
ENST00000329654.8:c.585-1008C>T	ENSP00000332116.4:n.585-1008C>T
ENST00000341517.8:c.585-1008C>T	ENSP00000342637.4:n.585-1008C>T
ENST00000371048.7:n.249-1008C>T
ENST00000412480.6:c.309-1008C>T	ENSP00000397548.2:n.309-1008C>T
ENST00000423207.6:c.540-1008C>T	ENSP00000392947.2:n.540-1008C>T
ENST00000490695.1:n.211-1008C>T
ENST00000491340.2:c.109-1008C>T
NM_001037340.2:c.540-1008C>T	NP_001032417.1:n.540-1008C>T
NM_001037341.1:c.585-1008C>T	NP_001032418.1:n.585-1008C>T
NM_001297440.1:c.309-1008C>T	NP_001284369.1:n.309-1008C>T
NM_001297441.1:c.360-1008C>T	NP_001284370.1:n.360-1008C>T
NM_002600.3:c.585-1008C>T	NP_002591.2:n.585-1008C>T
XM_011541565.1:c.321-1008C>T	XP_011539867.1:n.321-1008C>T
XM_011541566.1:c.16+7167C>T	XP_011539868.1:n.16+7167C>T
XM_017001445.1:c.168-1008C>T	XP_016856934.1:n.168-1008C>T
NM_002600.4:c.585-1008C>T MANE Select	NP_002591.2:n.585-1008C>T
NM_001037340.3:c.540-1008C>T	NP_001032417.1:n.540-1008C>T
NM_001037341.2:c.585-1008C>T	NP_001032418.1:n.585-1008C>T
NM_001297440.2:c.309-1008C>T	NP_001284369.1:n.309-1008C>T