Canonical Allele Identifier: CA1590817235

Gene: PDGFRB

Linked Data

• dbSNP Id: rs1761215177

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155775_150155777del , CM000667.2:g.150155775_150155777del	GRCh38
NC_000005.9:g.149535338_149535340del , CM000667.1:g.149535338_149535340del	GRCh37
NC_000005.8:g.149515531_149515533del	NCBI36
NG_023367.1:g.5086_5088del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-384_-382del MANE Select	ENSP00000261799.4:n.-384_-382del
ENST00000261799.8:c.-384_-382del	ENSP00000261799.4:n.-384_-382del
ENST00000517660.1:n.87_89del
ENST00000520579.5:c.-384_-382del	ENSP00000430026.1:n.-384_-382del
ENST00000523456.1:n.99_101del
NM_002609.3:c.-384_-382del	NP_002600.1:n.-384_-382del
XM_005268464.2:c.-530_-528del	XP_005268521.1:n.-530_-528del
XM_011537659.1:c.-851_-849del	XP_011535961.1:n.-851_-849del
NM_001355016.1:c.-530_-528del	NP_001341945.1:n.-530_-528del
NM_001355017.1:c.-901_-899del	NP_001341946.1:n.-901_-899del
NR_149150.1:n.86_88del
NM_002609.4:c.-384_-382del MANE Select	NP_002600.1:n.-384_-382del
NM_001355016.2:c.-530_-528del	NP_001341945.1:n.-530_-528del
NM_001355017.2:c.-901_-899del	NP_001341946.1:n.-901_-899del
NR_149150.2:n.72_74del