Canonical Allele Identifier: CA738007580

Gene: PDE4B

Linked Data

• dbSNP Id: rs1240285850
• gnomAD v3: 1-65845252-TTTG-T
• gnomAD v4: 1-65845252-TTTG-T
• MyVariant Identifiers: chr1:g.66310936_66310938del (hg19) ; chr1:g.65845253_65845255del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.65845256_65845258del , CM000663.2:g.65845256_65845258del	GRCh38
NC_000001.10:g.66310939_66310941del , CM000663.1:g.66310939_66310941del	GRCh37
NC_000001.9:g.66083527_66083529del	NCBI36
NG_029038.1:g.57747_57749del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341517.9:c.-71+52008_-71+52010del MANE Select	ENSP00000342637.4:n.-71+52008_-71+52010del
ENST00000329654.8:c.-71+52626_-71+52628del	ENSP00000332116.4:n.-71+52626_-71+52628del
ENST00000341517.8:c.-71+52008_-71+52010del	ENSP00000342637.4:n.-71+52008_-71+52010del
NM_001037341.1:c.-71+52626_-71+52628del	NP_001032418.1:n.-71+52626_-71+52628del
NM_001297440.1:c.-108+52626_-108+52628del	NP_001284369.1:n.-108+52626_-108+52628del
NM_002600.3:c.-71+52008_-71+52010del	NP_002591.2:n.-71+52008_-71+52010del
NM_002600.4:c.-71+52008_-71+52010del MANE Select	NP_002591.2:n.-71+52008_-71+52010del
NM_001037341.2:c.-71+52626_-71+52628del	NP_001032418.1:n.-71+52626_-71+52628del
NM_001297440.2:c.-108+52626_-108+52628del	NP_001284369.1:n.-108+52626_-108+52628del