Canonical Allele Identifier: CA1590817262

Gene: PDGFRB

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155841C= , CM000667.2:g.150155841C=	GRCh38
NC_000005.9:g.149535404C= , CM000667.1:g.149535404C=	GRCh37
NC_000005.8:g.149515597C=	NCBI36
NG_023367.1:g.5019G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-451G= MANE Select	ENSP00000261799.4:n.-451G=
ENST00000261799.8:c.-451G=	ENSP00000261799.4:n.-451G=
ENST00000517660.1:n.20G=
ENST00000520579.5:c.-451G=	ENSP00000430026.1:n.-451G=
ENST00000523456.1:n.32G=
NM_002609.3:c.-451G=	NP_002600.1:n.-451G=
XM_005268464.2:c.-597G=	XP_005268521.1:n.-597G=
XM_011537659.1:c.-918G=	XP_011535961.1:n.-918G=
NM_001355016.1:c.-597G=	NP_001341945.1:n.-597G=
NM_001355017.1:c.-968G=	NP_001341946.1:n.-968G=
NR_149150.1:n.19G=
NM_002609.4:c.-451G= MANE Select	NP_002600.1:n.-451G=
NM_001355016.2:c.-597G=	NP_001341945.1:n.-597G=
NM_001355017.2:c.-968G=	NP_001341946.1:n.-968G=
NR_149150.2:n.5G=