Canonical Allele Identifier: CA24399309

Gene: PDE4B

Linked Data

• dbSNP Id: rs537021379
• gnomAD v2: 1-66311005-G-A
• gnomAD v3: 1-65845322-G-A
• gnomAD v4: 1-65845322-G-A
• MyVariant Identifiers: chr1:g.66311005G>A (hg19) ; chr1:g.65845322G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.65845322G>A , CM000663.2:g.65845322G>A	GRCh38
NC_000001.10:g.66311005G>A , CM000663.1:g.66311005G>A	GRCh37
NC_000001.9:g.66083593G>A	NCBI36
NG_029038.1:g.57813G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341517.9:c.-71+52074G>A MANE Select	ENSP00000342637.4:n.-71+52074G>A
ENST00000329654.8:c.-71+52692G>A	ENSP00000332116.4:n.-71+52692G>A
ENST00000341517.8:c.-71+52074G>A	ENSP00000342637.4:n.-71+52074G>A
NM_001037341.1:c.-71+52692G>A	NP_001032418.1:n.-71+52692G>A
NM_001297440.1:c.-108+52692G>A	NP_001284369.1:n.-108+52692G>A
NM_002600.3:c.-71+52074G>A	NP_002591.2:n.-71+52074G>A
NM_002600.4:c.-71+52074G>A MANE Select	NP_002591.2:n.-71+52074G>A
NM_001037341.2:c.-71+52692G>A	NP_001032418.1:n.-71+52692G>A
NM_001297440.2:c.-108+52692G>A	NP_001284369.1:n.-108+52692G>A