Canonical Allele Identifier: CA2675968645

Gene: PDGFRB

Linked Data

• gnomAD v4: 5-150155809-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155809G>A , CM000667.2:g.150155809G>A	GRCh38
NC_000005.9:g.149535372G>A , CM000667.1:g.149535372G>A	GRCh37
NC_000005.8:g.149515565G>A	NCBI36
NG_023367.1:g.5051C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-419C>T MANE Select	ENSP00000261799.4:n.-419C>T
ENST00000261799.8:c.-419C>T	ENSP00000261799.4:n.-419C>T
ENST00000517660.1:n.52C>T
ENST00000520579.5:c.-419C>T	ENSP00000430026.1:n.-419C>T
ENST00000523456.1:n.64C>T
NM_002609.3:c.-419C>T	NP_002600.1:n.-419C>T
XM_005268464.2:c.-565C>T	XP_005268521.1:n.-565C>T
XM_011537659.1:c.-886C>T	XP_011535961.1:n.-886C>T
NM_001355016.1:c.-565C>T	NP_001341945.1:n.-565C>T
NM_001355017.1:c.-936C>T	NP_001341946.1:n.-936C>T
NR_149150.1:n.51C>T
NM_002609.4:c.-419C>T MANE Select	NP_002600.1:n.-419C>T
NM_001355016.2:c.-565C>T	NP_001341945.1:n.-565C>T
NM_001355017.2:c.-936C>T	NP_001341946.1:n.-936C>T
NR_149150.2:n.37C>T