Canonical Allele Identifier: CA2675968644

Gene: PDGFRB

Linked Data

• gnomAD v4: 5-150155808-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155811del , CM000667.2:g.150155811del	GRCh38
NC_000005.9:g.149535374del , CM000667.1:g.149535374del	GRCh37
NC_000005.8:g.149515567del	NCBI36
NG_023367.1:g.5051del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-419del MANE Select	ENSP00000261799.4:n.-419del
ENST00000261799.8:c.-419del	ENSP00000261799.4:n.-419del
ENST00000517660.1:n.52del
ENST00000520579.5:c.-419del	ENSP00000430026.1:n.-419del
ENST00000523456.1:n.64del
NM_002609.3:c.-419del	NP_002600.1:n.-419del
XM_005268464.2:c.-565del	XP_005268521.1:n.-565del
XM_011537659.1:c.-886del	XP_011535961.1:n.-886del
NM_001355016.1:c.-565del	NP_001341945.1:n.-565del
NM_001355017.1:c.-936del	NP_001341946.1:n.-936del
NR_149150.1:n.51del
NM_002609.4:c.-419del MANE Select	NP_002600.1:n.-419del
NM_001355016.2:c.-565del	NP_001341945.1:n.-565del
NM_001355017.2:c.-936del	NP_001341946.1:n.-936del
NR_149150.2:n.37del