Canonical Allele Identifier: CA1082866179

Gene: PDGFRB

Linked Data

• dbSNP Id: rs1761215114
• gnomAD v3: 5-150155770-A-T
• gnomAD v4: 5-150155770-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155770A>T , CM000667.2:g.150155770A>T	GRCh38
NC_000005.9:g.149535333A>T , CM000667.1:g.149535333A>T	GRCh37
NC_000005.8:g.149515526A>T	NCBI36
NG_023367.1:g.5090T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-380T>A MANE Select	ENSP00000261799.4:n.-380T>A
ENST00000261799.8:c.-380T>A	ENSP00000261799.4:n.-380T>A
ENST00000517660.1:n.91T>A
ENST00000520579.5:c.-380T>A	ENSP00000430026.1:n.-380T>A
ENST00000523456.1:n.103T>A
NM_002609.3:c.-380T>A	NP_002600.1:n.-380T>A
XM_005268464.2:c.-526T>A	XP_005268521.1:n.-526T>A
XM_011537659.1:c.-847T>A	XP_011535961.1:n.-847T>A
NM_001355016.1:c.-526T>A	NP_001341945.1:n.-526T>A
NM_001355017.1:c.-897T>A	NP_001341946.1:n.-897T>A
NR_149150.1:n.90T>A
NM_002609.4:c.-380T>A MANE Select	NP_002600.1:n.-380T>A
NM_001355016.2:c.-526T>A	NP_001341945.1:n.-526T>A
NM_001355017.2:c.-897T>A	NP_001341946.1:n.-897T>A
NR_149150.2:n.76T>A