Canonical Allele Identifier: CA1590817259

Gene: PDGFRB

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155833A= , CM000667.2:g.150155833A=	GRCh38
NC_000005.9:g.149535396A= , CM000667.1:g.149535396A=	GRCh37
NC_000005.8:g.149515589A=	NCBI36
NG_023367.1:g.5027T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-443T= MANE Select	ENSP00000261799.4:n.-443T=
ENST00000261799.8:c.-443T=	ENSP00000261799.4:n.-443T=
ENST00000517660.1:n.28T=
ENST00000520579.5:c.-443T=	ENSP00000430026.1:n.-443T=
ENST00000523456.1:n.40T=
NM_002609.3:c.-443T=	NP_002600.1:n.-443T=
XM_005268464.2:c.-589T=	XP_005268521.1:n.-589T=
XM_011537659.1:c.-910T=	XP_011535961.1:n.-910T=
NM_001355016.1:c.-589T=	NP_001341945.1:n.-589T=
NM_001355017.1:c.-960T=	NP_001341946.1:n.-960T=
NR_149150.1:n.27T=
NM_002609.4:c.-443T= MANE Select	NP_002600.1:n.-443T=
NM_001355016.2:c.-589T=	NP_001341945.1:n.-589T=
NM_001355017.2:c.-960T=	NP_001341946.1:n.-960T=
NR_149150.2:n.13T=