Canonical Allele Identifier: CA1590801613

Gene: PDGFRB

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150120840G= , CM000667.2:g.150120840G=	GRCh38
NC_000005.9:g.149500403G= , CM000667.1:g.149500403G=	GRCh37
NC_000005.8:g.149480596G=	NCBI36
NG_023367.1:g.40020C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.2586+48C= MANE Select	ENSP00000261799.4:n.2586+48C=
ENST00000261799.8:c.2586+48C=	ENSP00000261799.4:n.2586+48C=
ENST00000519575.5:n.500+48C=
ENST00000520579.5:c.*1900+48C=	ENSP00000430026.1:n.*1900+48C=
NM_002609.3:c.2586+48C=	NP_002600.1:n.2586+48C=
XM_005268464.2:c.2394+48C=	XP_005268521.1:n.2394+48C=
XM_011537658.1:c.2586+48C=	XP_011535960.1:n.2586+48C=
XM_011537659.1:c.2586+48C=	XP_011535961.1:n.2586+48C=
XM_011537660.1:c.2586+48C=	XP_011535962.1:n.2586+48C=
NM_001355016.1:c.2394+48C=	NP_001341945.1:n.2394+48C=
NM_001355017.1:c.2103+48C=	NP_001341946.1:n.2103+48C=
NM_002609.4:c.2586+48C= MANE Select	NP_002600.1:n.2586+48C=
NM_001355016.2:c.2394+48C=	NP_001341945.1:n.2394+48C=
NM_001355017.2:c.2103+48C=	NP_001341946.1:n.2103+48C=