Canonical Allele Identifier: CA2675968605

Gene: PDGFRB

Linked Data

• gnomAD v4: 5-150155772-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155772C>T , CM000667.2:g.150155772C>T	GRCh38
NC_000005.9:g.149535335C>T , CM000667.1:g.149535335C>T	GRCh37
NC_000005.8:g.149515528C>T	NCBI36
NG_023367.1:g.5088G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-382G>A MANE Select	ENSP00000261799.4:n.-382G>A
ENST00000261799.8:c.-382G>A	ENSP00000261799.4:n.-382G>A
ENST00000517660.1:n.89G>A
ENST00000520579.5:c.-382G>A	ENSP00000430026.1:n.-382G>A
ENST00000523456.1:n.101G>A
NM_002609.3:c.-382G>A	NP_002600.1:n.-382G>A
XM_005268464.2:c.-528G>A	XP_005268521.1:n.-528G>A
XM_011537659.1:c.-849G>A	XP_011535961.1:n.-849G>A
NM_001355016.1:c.-528G>A	NP_001341945.1:n.-528G>A
NM_001355017.1:c.-899G>A	NP_001341946.1:n.-899G>A
NR_149150.1:n.88G>A
NM_002609.4:c.-382G>A MANE Select	NP_002600.1:n.-382G>A
NM_001355016.2:c.-528G>A	NP_001341945.1:n.-528G>A
NM_001355017.2:c.-899G>A	NP_001341946.1:n.-899G>A
NR_149150.2:n.74G>A