Canonical Allele Identifier: CA805576777

Gene: PDGFRB

Linked Data

• dbSNP Id: rs1208896392
• MyVariant Identifiers: chr5:g.149535396_149535397insCTGCTGG (hg19) ; chr5:g.150155833_150155834insCTGCTGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155842_150155848dup , CM000667.2:g.150155842_150155848dup	GRCh38
NC_000005.9:g.149535405_149535411dup , CM000667.1:g.149535405_149535411dup	GRCh37
NC_000005.8:g.149515598_149515604dup	NCBI36
NG_023367.1:g.5020_5026dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.8:c.-450_-444dup	ENSP00000261799.4:n.-450_-444dup
ENST00000517660.1:n.21_27dup
ENST00000520579.5:c.-450_-444dup	ENSP00000430026.1:n.-450_-444dup
ENST00000523456.1:n.33_39dup
NM_002609.3:c.-450_-444dup	NP_002600.1:n.-450_-444dup
XM_005268464.2:c.-596_-590dup	XP_005268521.1:n.-596_-590dup
XM_011537659.1:c.-917_-911dup	XP_011535961.1:n.-917_-911dup
NM_001355016.1:c.-596_-590dup	NP_001341945.1:n.-596_-590dup
NM_001355017.1:c.-967_-961dup	NP_001341946.1:n.-967_-961dup
NR_149150.1:n.20_26dup