Canonical Allele Identifier: CA1172553496

Gene: PDE4B

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.66055315A>C , CM000663.2:g.66055315A>C	GRCh38
NC_000001.10:g.66520998A>C , CM000663.1:g.66520998A>C	GRCh37
NC_000001.9:g.66293586A>C	NCBI36
NG_029038.1:g.267806A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341517.9:c.281+136480A>C MANE Select	ENSP00000342637.4:n.281+136480A>C
ENST00000329654.8:c.281+136480A>C	ENSP00000332116.4:n.281+136480A>C
ENST00000341517.8:c.281+136480A>C	ENSP00000342637.4:n.281+136480A>C
ENST00000423207.6:c.236+62173A>C	ENSP00000392947.2:n.236+62173A>C
ENST00000526666.1:n.473+6425A>C
ENST00000531358.1:n.528-57455A>C
ENST00000532040.1:n.409-7579A>C
NM_001037340.2:c.236+62173A>C	NP_001032417.1:n.236+62173A>C
NM_001037341.1:c.281+136480A>C	NP_001032418.1:n.281+136480A>C
NM_001297440.1:c.5+141959A>C	NP_001284369.1:n.5+141959A>C
NM_001297441.1:c.56+14607A>C	NP_001284370.1:n.56+14607A>C
NM_002600.3:c.281+136480A>C	NP_002591.2:n.281+136480A>C
XM_011541565.1:c.17+6425A>C	XP_011539867.1:n.17+6425A>C
XM_011541566.1:c.-288+136480A>C	XP_011539868.1:n.-288+136480A>C
NM_002600.4:c.281+136480A>C MANE Select	NP_002591.2:n.281+136480A>C
NM_001037340.3:c.236+62173A>C	NP_001032417.1:n.236+62173A>C
NM_001037341.2:c.281+136480A>C	NP_001032418.1:n.281+136480A>C
NM_001297440.2:c.5+141959A>C	NP_001284369.1:n.5+141959A>C