Canonical Allele Identifier: CA1082866230

Gene: PDGFRB

Linked Data

• dbSNP Id: rs1761215311
• gnomAD v3: 5-150155773-TC-T
• gnomAD v4: 5-150155773-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155775del , CM000667.2:g.150155775del	GRCh38
NC_000005.9:g.149535338del , CM000667.1:g.149535338del	GRCh37
NC_000005.8:g.149515531del	NCBI36
NG_023367.1:g.5086del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-384del MANE Select	ENSP00000261799.4:n.-384del
ENST00000261799.8:c.-384del	ENSP00000261799.4:n.-384del
ENST00000517660.1:n.87del
ENST00000520579.5:c.-384del	ENSP00000430026.1:n.-384del
ENST00000523456.1:n.99del
NM_002609.3:c.-384del	NP_002600.1:n.-384del
XM_005268464.2:c.-530del	XP_005268521.1:n.-530del
XM_011537659.1:c.-851del	XP_011535961.1:n.-851del
NM_001355016.1:c.-530del	NP_001341945.1:n.-530del
NM_001355017.1:c.-901del	NP_001341946.1:n.-901del
NR_149150.1:n.86del
NM_002609.4:c.-384del MANE Select	NP_002600.1:n.-384del
NM_001355016.2:c.-530del	NP_001341945.1:n.-530del
NM_001355017.2:c.-901del	NP_001341946.1:n.-901del
NR_149150.2:n.72del