Canonical Allele Identifier: CA1590817256

Gene: PDGFRB

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155826G= , CM000667.2:g.150155826G=	GRCh38
NC_000005.9:g.149535389G= , CM000667.1:g.149535389G=	GRCh37
NC_000005.8:g.149515582G=	NCBI36
NG_023367.1:g.5034C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-436C= MANE Select	ENSP00000261799.4:n.-436C=
ENST00000261799.8:c.-436C=	ENSP00000261799.4:n.-436C=
ENST00000517660.1:n.35C=
ENST00000520579.5:c.-436C=	ENSP00000430026.1:n.-436C=
ENST00000523456.1:n.47C=
NM_002609.3:c.-436C=	NP_002600.1:n.-436C=
XM_005268464.2:c.-582C=	XP_005268521.1:n.-582C=
XM_011537659.1:c.-903C=	XP_011535961.1:n.-903C=
NM_001355016.1:c.-582C=	NP_001341945.1:n.-582C=
NM_001355017.1:c.-953C=	NP_001341946.1:n.-953C=
NR_149150.1:n.34C=
NM_002609.4:c.-436C= MANE Select	NP_002600.1:n.-436C=
NM_001355016.2:c.-582C=	NP_001341945.1:n.-582C=
NM_001355017.2:c.-953C=	NP_001341946.1:n.-953C=
NR_149150.2:n.20C=