Canonical Allele Identifier: CA24399300

Gene: PDE4B

Linked Data

• dbSNP Id: rs967285979
• gnomAD v3: 1-65845220-T-G
• gnomAD v4: 1-65845220-T-G
• MyVariant Identifiers: chr1:g.66310903T>G (hg19) ; chr1:g.65845220T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.65845220T>G , CM000663.2:g.65845220T>G	GRCh38
NC_000001.10:g.66310903T>G , CM000663.1:g.66310903T>G	GRCh37
NC_000001.9:g.66083491T>G	NCBI36
NG_029038.1:g.57711T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000341517.9:c.-71+51972T>G MANE Select	ENSP00000342637.4:n.-71+51972T>G
ENST00000329654.8:c.-71+52590T>G	ENSP00000332116.4:n.-71+52590T>G
ENST00000341517.8:c.-71+51972T>G	ENSP00000342637.4:n.-71+51972T>G
NM_001037341.1:c.-71+52590T>G	NP_001032418.1:n.-71+52590T>G
NM_001297440.1:c.-108+52590T>G	NP_001284369.1:n.-108+52590T>G
NM_002600.3:c.-71+51972T>G	NP_002591.2:n.-71+51972T>G
NM_002600.4:c.-71+51972T>G MANE Select	NP_002591.2:n.-71+51972T>G
NM_001037341.2:c.-71+52590T>G	NP_001032418.1:n.-71+52590T>G
NM_001297440.2:c.-108+52590T>G	NP_001284369.1:n.-108+52590T>G