Canonical Allele Identifier: CA1590801605

Gene: PDGFRB

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150120830C= , CM000667.2:g.150120830C=	GRCh38
NC_000005.9:g.149500393C= , CM000667.1:g.149500393C=	GRCh37
NC_000005.8:g.149480586C=	NCBI36
NG_023367.1:g.40030G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.2586+58G= MANE Select	ENSP00000261799.4:n.2586+58G=
ENST00000261799.8:c.2586+58G=	ENSP00000261799.4:n.2586+58G=
ENST00000519575.5:n.500+58G=
ENST00000520579.5:c.*1900+58G=	ENSP00000430026.1:n.*1900+58G=
NM_002609.3:c.2586+58G=	NP_002600.1:n.2586+58G=
XM_005268464.2:c.2394+58G=	XP_005268521.1:n.2394+58G=
XM_011537658.1:c.2586+58G=	XP_011535960.1:n.2586+58G=
XM_011537659.1:c.2586+58G=	XP_011535961.1:n.2586+58G=
XM_011537660.1:c.2586+58G=	XP_011535962.1:n.2586+58G=
NM_001355016.1:c.2394+58G=	NP_001341945.1:n.2394+58G=
NM_001355017.1:c.2103+58G=	NP_001341946.1:n.2103+58G=
NM_002609.4:c.2586+58G= MANE Select	NP_002600.1:n.2586+58G=
NM_001355016.2:c.2394+58G=	NP_001341945.1:n.2394+58G=
NM_001355017.2:c.2103+58G=	NP_001341946.1:n.2103+58G=