Canonical Allele Identifier: CA1590805613

Gene: PDGFRB

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150129773G= , CM000667.2:g.150129773G=	GRCh38
NC_000005.9:g.149509336G= , CM000667.1:g.149509336G=	GRCh37
NC_000005.8:g.149489529G=	NCBI36
NG_023367.1:g.31087C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261799.9:c.1563C= MANE Select	ENSP00000261799.4:p.Val521=
ENST00000261799.8:c.1563C=	ENSP00000261799.4:p.Val521=
ENST00000520579.5:c.*877C=	ENSP00000430026.1:n.*877C=
NM_002609.3:c.1563C=	NP_002600.1:p.Val521=
XM_005268464.2:c.1371C=	XP_005268521.1:p.Val457=
XM_011537658.1:c.1563C=	XP_011535960.1:p.Val521=
XM_011537659.1:c.1563C=	XP_011535961.1:p.Val521=
XM_011537660.1:c.1563C=	XP_011535962.1:p.Val521=
NM_001355016.1:c.1371C=	NP_001341945.1:p.Val457=
NM_001355017.1:c.1080C=	NP_001341946.1:p.Val360=
NM_002609.4:c.1563C= MANE Select	NP_002600.1:p.Val521=
NM_001355016.2:c.1371C=	NP_001341945.1:p.Val457=
NM_001355017.2:c.1080C=	NP_001341946.1:p.Val360=