Canonical Allele Identifier: CA2572200449

Gene: PDGFRB

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155777C>T , CM000667.2:g.150155777C>T	GRCh38
NC_000005.9:g.149535340C>T , CM000667.1:g.149535340C>T	GRCh37
NC_000005.8:g.149515533C>T	NCBI36
NG_023367.1:g.5083G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-387G>A MANE Select	ENSP00000261799.4:n.-387G>A
ENST00000261799.8:c.-387G>A	ENSP00000261799.4:n.-387G>A
ENST00000517660.1:n.84G>A
ENST00000520579.5:c.-387G>A	ENSP00000430026.1:n.-387G>A
ENST00000523456.1:n.96G>A
NM_002609.3:c.-387G>A	NP_002600.1:n.-387G>A
XM_005268464.2:c.-533G>A	XP_005268521.1:n.-533G>A
XM_011537659.1:c.-854G>A	XP_011535961.1:n.-854G>A
NM_001355016.1:c.-533G>A	NP_001341945.1:n.-533G>A
NM_001355017.1:c.-904G>A	NP_001341946.1:n.-904G>A
NR_149150.1:n.83G>A
NM_002609.4:c.-387G>A MANE Select	NP_002600.1:n.-387G>A
NM_001355016.2:c.-533G>A	NP_001341945.1:n.-533G>A
NM_001355017.2:c.-904G>A	NP_001341946.1:n.-904G>A
NR_149150.2:n.69G>A