Canonical Allele Identifier: CA805576751

Gene: PDGFRB

Linked Data

• dbSNP Id: rs1286386193
• MyVariant Identifiers: chr5:g.149535330T>A (hg19) ; chr5:g.150155767T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155767T>A , CM000667.2:g.150155767T>A	GRCh38
NC_000005.9:g.149535330T>A , CM000667.1:g.149535330T>A	GRCh37
NC_000005.8:g.149515523T>A	NCBI36
NG_023367.1:g.5093A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-377A>T MANE Select	ENSP00000261799.4:n.-377A>T
ENST00000261799.8:c.-377A>T	ENSP00000261799.4:n.-377A>T
ENST00000517660.1:n.94A>T
ENST00000520579.5:c.-377A>T	ENSP00000430026.1:n.-377A>T
ENST00000523456.1:n.106A>T
NM_002609.3:c.-377A>T	NP_002600.1:n.-377A>T
XM_005268464.2:c.-523A>T	XP_005268521.1:n.-523A>T
XM_011537659.1:c.-844A>T	XP_011535961.1:n.-844A>T
NM_001355016.1:c.-523A>T	NP_001341945.1:n.-523A>T
NM_001355017.1:c.-894A>T	NP_001341946.1:n.-894A>T
NR_149150.1:n.93A>T
NM_002609.4:c.-377A>T MANE Select	NP_002600.1:n.-377A>T
NM_001355016.2:c.-523A>T	NP_001341945.1:n.-523A>T
NM_001355017.2:c.-894A>T	NP_001341946.1:n.-894A>T
NR_149150.2:n.79A>T