Canonical Allele Identifier: CA2675968669

Gene: PDGFRB

Linked Data

• gnomAD v4: 5-150155831-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155831T>C , CM000667.2:g.150155831T>C	GRCh38
NC_000005.9:g.149535394T>C , CM000667.1:g.149535394T>C	GRCh37
NC_000005.8:g.149515587T>C	NCBI36
NG_023367.1:g.5029A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-441A>G MANE Select	ENSP00000261799.4:n.-441A>G
ENST00000261799.8:c.-441A>G	ENSP00000261799.4:n.-441A>G
ENST00000517660.1:n.30A>G
ENST00000520579.5:c.-441A>G	ENSP00000430026.1:n.-441A>G
ENST00000523456.1:n.42A>G
NM_002609.3:c.-441A>G	NP_002600.1:n.-441A>G
XM_005268464.2:c.-587A>G	XP_005268521.1:n.-587A>G
XM_011537659.1:c.-908A>G	XP_011535961.1:n.-908A>G
NM_001355016.1:c.-587A>G	NP_001341945.1:n.-587A>G
NM_001355017.1:c.-958A>G	NP_001341946.1:n.-958A>G
NR_149150.1:n.29A>G
NM_002609.4:c.-441A>G MANE Select	NP_002600.1:n.-441A>G
NM_001355016.2:c.-587A>G	NP_001341945.1:n.-587A>G
NM_001355017.2:c.-958A>G	NP_001341946.1:n.-958A>G
NR_149150.2:n.15A>G