Canonical Allele Identifier: CA738007522

Gene: PDE4B

Linked Data

• dbSNP Id: rs1331327215
• gnomAD v3: 1-65845156-C-T
• gnomAD v4: 1-65845156-C-T
• MyVariant Identifiers: chr1:g.66310839C>T (hg19) ; chr1:g.65845156C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.65845156C>T , CM000663.2:g.65845156C>T	GRCh38
NC_000001.10:g.66310839C>T , CM000663.1:g.66310839C>T	GRCh37
NC_000001.9:g.66083427C>T	NCBI36
NG_029038.1:g.57647C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341517.9:c.-71+51908C>T MANE Select	ENSP00000342637.4:n.-71+51908C>T
ENST00000329654.8:c.-71+52526C>T	ENSP00000332116.4:n.-71+52526C>T
ENST00000341517.8:c.-71+51908C>T	ENSP00000342637.4:n.-71+51908C>T
NM_001037341.1:c.-71+52526C>T	NP_001032418.1:n.-71+52526C>T
NM_001297440.1:c.-108+52526C>T	NP_001284369.1:n.-108+52526C>T
NM_002600.3:c.-71+51908C>T	NP_002591.2:n.-71+51908C>T
NM_002600.4:c.-71+51908C>T MANE Select	NP_002591.2:n.-71+51908C>T
NM_001037341.2:c.-71+52526C>T	NP_001032418.1:n.-71+52526C>T
NM_001297440.2:c.-108+52526C>T	NP_001284369.1:n.-108+52526C>T