Canonical Allele Identifier: CA2768885179

Gene: PDGFRB

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155840del , CM000667.2:g.150155840del	GRCh38
NC_000005.9:g.149535403del , CM000667.1:g.149535403del	GRCh37
NC_000005.8:g.149515596del	NCBI36
NG_023367.1:g.5021del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-449del MANE Select	ENSP00000261799.4:n.-449del
ENST00000261799.8:c.-449del	ENSP00000261799.4:n.-449del
ENST00000517660.1:n.22del
ENST00000520579.5:c.-449del	ENSP00000430026.1:n.-449del
ENST00000523456.1:n.34del
NM_002609.3:c.-449del	NP_002600.1:n.-449del
XM_005268464.2:c.-595del	XP_005268521.1:n.-595del
XM_011537659.1:c.-916del	XP_011535961.1:n.-916del
NM_001355016.1:c.-595del	NP_001341945.1:n.-595del
NM_001355017.1:c.-966del	NP_001341946.1:n.-966del
NR_149150.1:n.21del
NM_002609.4:c.-449del MANE Select	NP_002600.1:n.-449del
NM_001355016.2:c.-595del	NP_001341945.1:n.-595del
NM_001355017.2:c.-966del	NP_001341946.1:n.-966del
NR_149150.2:n.7del