Canonical Allele Identifier: CA1590803136
Gene: PDGFRB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150124300A= , CM000667.2:g.150124300A= GRCh38
NC_000005.9:g.149503863A= , CM000667.1:g.149503863A= GRCh37
NC_000005.8:g.149484056A= NCBI36
NG_023367.1:g.36560T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261799.9:c.1973T= MANE Select ENSP00000261799.4:p.Leu658=
ENST00000261799.8:c.1973T= ENSP00000261799.4:p.Leu658=
ENST00000520229.1:n.608T=
ENST00000520579.5:c.*1287T= ENSP00000430026.1:n.*1287T=
NM_002609.3:c.1973T= NP_002600.1:p.Leu658=
XM_005268464.2:c.1781T= XP_005268521.1:p.Leu594=
XM_011537658.1:c.1973T= XP_011535960.1:p.Leu658=
XM_011537659.1:c.1973T= XP_011535961.1:p.Leu658=
XM_011537660.1:c.1973T= XP_011535962.1:p.Leu658=
NM_001355016.1:c.1781T= NP_001341945.1:p.Leu594=
NM_001355017.1:c.1490T= NP_001341946.1:p.Leu497=
NM_002609.4:c.1973T= MANE Select NP_002600.1:p.Leu658=
NM_001355016.2:c.1781T= NP_001341945.1:p.Leu594=
NM_001355017.2:c.1490T= NP_001341946.1:p.Leu497=