Canonical Allele Identifier: CA2675968621

Gene: PDGFRB

Linked Data

• gnomAD v4: 5-150155787-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155787A>G , CM000667.2:g.150155787A>G	GRCh38
NC_000005.9:g.149535350A>G , CM000667.1:g.149535350A>G	GRCh37
NC_000005.8:g.149515543A>G	NCBI36
NG_023367.1:g.5073T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-397T>C MANE Select	ENSP00000261799.4:n.-397T>C
ENST00000261799.8:c.-397T>C	ENSP00000261799.4:n.-397T>C
ENST00000517660.1:n.74T>C
ENST00000520579.5:c.-397T>C	ENSP00000430026.1:n.-397T>C
ENST00000523456.1:n.86T>C
NM_002609.3:c.-397T>C	NP_002600.1:n.-397T>C
XM_005268464.2:c.-543T>C	XP_005268521.1:n.-543T>C
XM_011537659.1:c.-864T>C	XP_011535961.1:n.-864T>C
NM_001355016.1:c.-543T>C	NP_001341945.1:n.-543T>C
NM_001355017.1:c.-914T>C	NP_001341946.1:n.-914T>C
NR_149150.1:n.73T>C
NM_002609.4:c.-397T>C MANE Select	NP_002600.1:n.-397T>C
NM_001355016.2:c.-543T>C	NP_001341945.1:n.-543T>C
NM_001355017.2:c.-914T>C	NP_001341946.1:n.-914T>C
NR_149150.2:n.59T>C