Canonical Allele Identifier: CA1590817261

Gene: PDGFRB

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155839G= , CM000667.2:g.150155839G=	GRCh38
NC_000005.9:g.149535402G= , CM000667.1:g.149535402G=	GRCh37
NC_000005.8:g.149515595G=	NCBI36
NG_023367.1:g.5021C=

Transcript Alleles

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