Canonical Allele Identifier: CA2675968639

Gene: PDGFRB

Linked Data

• gnomAD v4: 5-150155805-TCCTGGGTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155808_150155815del , CM000667.2:g.150155808_150155815del	GRCh38
NC_000005.9:g.149535371_149535378del , CM000667.1:g.149535371_149535378del	GRCh37
NC_000005.8:g.149515564_149515571del	NCBI36
NG_023367.1:g.5047_5054del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-423_-416del MANE Select	ENSP00000261799.4:n.-423_-416del
ENST00000261799.8:c.-423_-416del	ENSP00000261799.4:n.-423_-416del
ENST00000517660.1:n.48_55del
ENST00000520579.5:c.-423_-416del	ENSP00000430026.1:n.-423_-416del
ENST00000523456.1:n.60_67del
NM_002609.3:c.-423_-416del	NP_002600.1:n.-423_-416del
XM_005268464.2:c.-569_-562del	XP_005268521.1:n.-569_-562del
XM_011537659.1:c.-890_-883del	XP_011535961.1:n.-890_-883del
NM_001355016.1:c.-569_-562del	NP_001341945.1:n.-569_-562del
NM_001355017.1:c.-940_-933del	NP_001341946.1:n.-940_-933del
NR_149150.1:n.47_54del
NM_002609.4:c.-423_-416del MANE Select	NP_002600.1:n.-423_-416del
NM_001355016.2:c.-569_-562del	NP_001341945.1:n.-569_-562del
NM_001355017.2:c.-940_-933del	NP_001341946.1:n.-940_-933del
NR_149150.2:n.33_40del