Canonical Allele Identifier: CA361714889

Gene: PDGFRB

Linked Data

• MyVariant Identifiers: chr5:g.149509435C>A (hg19) ; chr5:g.150129872C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150129872C>A , CM000667.2:g.150129872C>A	GRCh38
NC_000005.9:g.149509435C>A , CM000667.1:g.149509435C>A	GRCh37
NC_000005.8:g.149489628C>A	NCBI36
NG_023367.1:g.30988G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261799.9:c.1464G>T MANE Select	ENSP00000261799.4:p.Glu488Asp
ENST00000261799.8:c.1464G>T	ENSP00000261799.4:p.Glu488Asp
ENST00000520579.5:c.*778G>T	ENSP00000430026.1:n.*778G>T
NM_002609.3:c.1464G>T	NP_002600.1:p.Glu488Asp
XM_005268464.2:c.1272G>T	XP_005268521.1:p.Glu424Asp
XM_011537658.1:c.1464G>T	XP_011535960.1:p.Glu488Asp
XM_011537659.1:c.1464G>T	XP_011535961.1:p.Glu488Asp
XM_011537660.1:c.1464G>T	XP_011535962.1:p.Glu488Asp
NM_001355016.1:c.1272G>T	NP_001341945.1:p.Glu424Asp
NM_001355017.1:c.981G>T	NP_001341946.1:p.Glu327Asp
NM_002609.4:c.1464G>T MANE Select	NP_002600.1:p.Glu488Asp
NM_001355016.2:c.1272G>T	NP_001341945.1:p.Glu424Asp
NM_001355017.2:c.981G>T	NP_001341946.1:p.Glu327Asp