Canonical Allele Identifier: CA1590802605
Gene: PDGFRB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150123142G= , CM000667.2:g.150123142G= GRCh38
NC_000005.9:g.149502705G= , CM000667.1:g.149502705G= GRCh37
NC_000005.8:g.149482898G= NCBI36
NG_023367.1:g.37718C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261799.9:c.2083C= MANE Select ENSP00000261799.4:p.Arg695=
ENST00000261799.8:c.2083C= ENSP00000261799.4:p.Arg695=
ENST00000520579.5:c.*1397C= ENSP00000430026.1:n.*1397C=
NM_002609.3:c.2083C= NP_002600.1:p.Arg695=
XM_005268464.2:c.1891C= XP_005268521.1:p.Arg631=
XM_011537658.1:c.2083C= XP_011535960.1:p.Arg695=
XM_011537659.1:c.2083C= XP_011535961.1:p.Arg695=
XM_011537660.1:c.2083C= XP_011535962.1:p.Arg695=
NM_001355016.1:c.1891C= NP_001341945.1:p.Arg631=
NM_001355017.1:c.1600C= NP_001341946.1:p.Arg534=
NM_002609.4:c.2083C= MANE Select NP_002600.1:p.Arg695=
NM_001355016.2:c.1891C= NP_001341945.1:p.Arg631=
NM_001355017.2:c.1600C= NP_001341946.1:p.Arg534=