Canonical Allele Identifier: CA24449657

Gene: PDE4B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.66303417G>C , CM000663.2:g.66303417G>C	GRCh38
NC_000001.10:g.66769100G>C , CM000663.1:g.66769100G>C	GRCh37
NC_000001.9:g.66541688G>C	NCBI36
NG_029038.1:g.515908G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341517.9:c.635-29091G>C MANE Select	ENSP00000342637.4:n.635-29091G>C
ENST00000329654.8:c.635-29091G>C	ENSP00000332116.4:n.635-29091G>C
ENST00000341517.8:c.635-29091G>C	ENSP00000342637.4:n.635-29091G>C
ENST00000412480.6:c.359-29091G>C	ENSP00000397548.2:n.359-29091G>C
ENST00000423207.6:c.590-29091G>C	ENSP00000392947.2:n.590-29091G>C
NM_001037340.2:c.590-29091G>C	NP_001032417.1:n.590-29091G>C
NM_001037341.1:c.635-29091G>C	NP_001032418.1:n.635-29091G>C
NM_001297440.1:c.359-29091G>C	NP_001284369.1:n.359-29091G>C
NM_001297441.1:c.410-29091G>C	NP_001284370.1:n.410-29091G>C
NM_002600.3:c.635-29091G>C	NP_002591.2:n.635-29091G>C
XM_011541565.1:c.371-29091G>C	XP_011539867.1:n.371-29091G>C
XM_011541566.1:c.17-29091G>C	XP_011539868.1:n.17-29091G>C
XM_017001445.1:c.218-29091G>C	XP_016856934.1:n.218-29091G>C
NM_002600.4:c.635-29091G>C MANE Select	NP_002591.2:n.635-29091G>C
NM_001037340.3:c.590-29091G>C	NP_001032417.1:n.590-29091G>C
NM_001037341.2:c.635-29091G>C	NP_001032418.1:n.635-29091G>C
NM_001297440.2:c.359-29091G>C	NP_001284369.1:n.359-29091G>C