Canonical Allele Identifier: CA2675968632

Gene: PDGFRB

Linked Data

• gnomAD v4: 5-150155798-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155798A>C , CM000667.2:g.150155798A>C	GRCh38
NC_000005.9:g.149535361A>C , CM000667.1:g.149535361A>C	GRCh37
NC_000005.8:g.149515554A>C	NCBI36
NG_023367.1:g.5062T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-408T>G MANE Select	ENSP00000261799.4:n.-408T>G
ENST00000261799.8:c.-408T>G	ENSP00000261799.4:n.-408T>G
ENST00000517660.1:n.63T>G
ENST00000520579.5:c.-408T>G	ENSP00000430026.1:n.-408T>G
ENST00000523456.1:n.75T>G
NM_002609.3:c.-408T>G	NP_002600.1:n.-408T>G
XM_005268464.2:c.-554T>G	XP_005268521.1:n.-554T>G
XM_011537659.1:c.-875T>G	XP_011535961.1:n.-875T>G
NM_001355016.1:c.-554T>G	NP_001341945.1:n.-554T>G
NM_001355017.1:c.-925T>G	NP_001341946.1:n.-925T>G
NR_149150.1:n.62T>G
NM_002609.4:c.-408T>G MANE Select	NP_002600.1:n.-408T>G
NM_001355016.2:c.-554T>G	NP_001341945.1:n.-554T>G
NM_001355017.2:c.-925T>G	NP_001341946.1:n.-925T>G
NR_149150.2:n.48T>G