Canonical Allele Identifier: CA361714903

Gene: PDGFRB

Linked Data

• dbSNP Id: rs1760409279
• MyVariant Identifiers: chr5:g.149509440G>A (hg19) ; chr5:g.150129877G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150129877G>A , CM000667.2:g.150129877G>A	GRCh38
NC_000005.9:g.149509440G>A , CM000667.1:g.149509440G>A	GRCh37
NC_000005.8:g.149489633G>A	NCBI36
NG_023367.1:g.30983C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261799.9:c.1459C>T MANE Select	ENSP00000261799.4:p.Gln487Ter
ENST00000261799.8:c.1459C>T	ENSP00000261799.4:p.Gln487Ter
ENST00000520579.5:c.*773C>T	ENSP00000430026.1:n.*773C>T
NM_002609.3:c.1459C>T	NP_002600.1:p.Gln487Ter
XM_005268464.2:c.1267C>T	XP_005268521.1:p.Gln423Ter
XM_011537658.1:c.1459C>T	XP_011535960.1:p.Gln487Ter
XM_011537659.1:c.1459C>T	XP_011535961.1:p.Gln487Ter
XM_011537660.1:c.1459C>T	XP_011535962.1:p.Gln487Ter
NM_001355016.1:c.1267C>T	NP_001341945.1:p.Gln423Ter
NM_001355017.1:c.976C>T	NP_001341946.1:p.Gln326Ter
NM_002609.4:c.1459C>T MANE Select	NP_002600.1:p.Gln487Ter
NM_001355016.2:c.1267C>T	NP_001341945.1:p.Gln423Ter
NM_001355017.2:c.976C>T	NP_001341946.1:p.Gln326Ter