Canonical Allele Identifier: CA129082511

Gene: PDGFRB

Linked Data

• dbSNP Id: rs754955253
• gnomAD v4: 5-150155774-CCT-C
• MyVariant Identifiers: chr5:g.149535338_149535339del (hg19) ; chr5:g.150155775_150155776del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155779_150155780del , CM000667.2:g.150155779_150155780del	GRCh38
NC_000005.9:g.149535342_149535343del , CM000667.1:g.149535342_149535343del	GRCh37
NC_000005.8:g.149515535_149515536del	NCBI36
NG_023367.1:g.5084_5085del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-386_-385del MANE Select	ENSP00000261799.4:n.-386_-385del
ENST00000261799.8:c.-386_-385del	ENSP00000261799.4:n.-386_-385del
ENST00000517660.1:n.85_86del
ENST00000520579.5:c.-386_-385del	ENSP00000430026.1:n.-386_-385del
ENST00000523456.1:n.97_98del
NM_002609.3:c.-386_-385del	NP_002600.1:n.-386_-385del
XM_005268464.2:c.-532_-531del	XP_005268521.1:n.-532_-531del
XM_011537659.1:c.-853_-852del	XP_011535961.1:n.-853_-852del
NM_001355016.1:c.-532_-531del	NP_001341945.1:n.-532_-531del
NM_001355017.1:c.-903_-902del	NP_001341946.1:n.-903_-902del
NR_149150.1:n.84_85del
NM_002609.4:c.-386_-385del MANE Select	NP_002600.1:n.-386_-385del
NM_001355016.2:c.-532_-531del	NP_001341945.1:n.-532_-531del
NM_001355017.2:c.-903_-902del	NP_001341946.1:n.-903_-902del
NR_149150.2:n.70_71del