Canonical Allele Identifier: CA24399295

Gene: PDE4B

Linked Data

• dbSNP Id: rs1034419829
• MyVariant Identifiers: chr1:g.66310870A>C (hg19) ; chr1:g.65845187A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.65845187A>C , CM000663.2:g.65845187A>C	GRCh38
NC_000001.10:g.66310870A>C , CM000663.1:g.66310870A>C	GRCh37
NC_000001.9:g.66083458A>C	NCBI36
NG_029038.1:g.57678A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000341517.9:c.-71+51939A>C MANE Select	ENSP00000342637.4:n.-71+51939A>C
ENST00000329654.8:c.-71+52557A>C	ENSP00000332116.4:n.-71+52557A>C
ENST00000341517.8:c.-71+51939A>C	ENSP00000342637.4:n.-71+51939A>C
NM_001037341.1:c.-71+52557A>C	NP_001032418.1:n.-71+52557A>C
NM_001297440.1:c.-108+52557A>C	NP_001284369.1:n.-108+52557A>C
NM_002600.3:c.-71+51939A>C	NP_002591.2:n.-71+51939A>C
NM_002600.4:c.-71+51939A>C MANE Select	NP_002591.2:n.-71+51939A>C
NM_001037341.2:c.-71+52557A>C	NP_001032418.1:n.-71+52557A>C
NM_001297440.2:c.-108+52557A>C	NP_001284369.1:n.-108+52557A>C