Canonical Allele Identifier: CA1590817239

Gene: PDGFRB

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155775C= , CM000667.2:g.150155775C=	GRCh38
NC_000005.9:g.149535338C= , CM000667.1:g.149535338C=	GRCh37
NC_000005.8:g.149515531C=	NCBI36
NG_023367.1:g.5085G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-385G= MANE Select	ENSP00000261799.4:n.-385G=
ENST00000261799.8:c.-385G=	ENSP00000261799.4:n.-385G=
ENST00000517660.1:n.86G=
ENST00000520579.5:c.-385G=	ENSP00000430026.1:n.-385G=
ENST00000523456.1:n.98G=
NM_002609.3:c.-385G=	NP_002600.1:n.-385G=
XM_005268464.2:c.-531G=	XP_005268521.1:n.-531G=
XM_011537659.1:c.-852G=	XP_011535961.1:n.-852G=
NM_001355016.1:c.-531G=	NP_001341945.1:n.-531G=
NM_001355017.1:c.-902G=	NP_001341946.1:n.-902G=
NR_149150.1:n.85G=
NM_002609.4:c.-385G= MANE Select	NP_002600.1:n.-385G=
NM_001355016.2:c.-531G=	NP_001341945.1:n.-531G=
NM_001355017.2:c.-902G=	NP_001341946.1:n.-902G=
NR_149150.2:n.71G=