Canonical Allele Identifier: CA2675968635

Gene: PDGFRB

Linked Data

• gnomAD v4: 5-150155799-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155799G>A , CM000667.2:g.150155799G>A	GRCh38
NC_000005.9:g.149535362G>A , CM000667.1:g.149535362G>A	GRCh37
NC_000005.8:g.149515555G>A	NCBI36
NG_023367.1:g.5061C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-409C>T MANE Select	ENSP00000261799.4:n.-409C>T
ENST00000261799.8:c.-409C>T	ENSP00000261799.4:n.-409C>T
ENST00000517660.1:n.62C>T
ENST00000520579.5:c.-409C>T	ENSP00000430026.1:n.-409C>T
ENST00000523456.1:n.74C>T
NM_002609.3:c.-409C>T	NP_002600.1:n.-409C>T
XM_005268464.2:c.-555C>T	XP_005268521.1:n.-555C>T
XM_011537659.1:c.-876C>T	XP_011535961.1:n.-876C>T
NM_001355016.1:c.-555C>T	NP_001341945.1:n.-555C>T
NM_001355017.1:c.-926C>T	NP_001341946.1:n.-926C>T
NR_149150.1:n.61C>T
NM_002609.4:c.-409C>T MANE Select	NP_002600.1:n.-409C>T
NM_001355016.2:c.-555C>T	NP_001341945.1:n.-555C>T
NM_001355017.2:c.-926C>T	NP_001341946.1:n.-926C>T
NR_149150.2:n.47C>T