Canonical Allele Identifier: CA2743944507

Gene: PDE4B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.65845183T>C , CM000663.2:g.65845183T>C	GRCh38
NC_000001.10:g.66310866T>C , CM000663.1:g.66310866T>C	GRCh37
NC_000001.9:g.66083454T>C	NCBI36
NG_029038.1:g.57674T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341517.9:c.-71+51935T>C MANE Select	ENSP00000342637.4:n.-71+51935T>C
ENST00000329654.8:c.-71+52553T>C	ENSP00000332116.4:n.-71+52553T>C
ENST00000341517.8:c.-71+51935T>C	ENSP00000342637.4:n.-71+51935T>C
NM_001037341.1:c.-71+52553T>C	NP_001032418.1:n.-71+52553T>C
NM_001297440.1:c.-108+52553T>C	NP_001284369.1:n.-108+52553T>C
NM_002600.3:c.-71+51935T>C	NP_002591.2:n.-71+51935T>C
NM_002600.4:c.-71+51935T>C MANE Select	NP_002591.2:n.-71+51935T>C
NM_001037341.2:c.-71+52553T>C	NP_001032418.1:n.-71+52553T>C
NM_001297440.2:c.-108+52553T>C	NP_001284369.1:n.-108+52553T>C