Canonical Allele Identifier: CA1590817248
Gene: PDGFRB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150155804A= , CM000667.2:g.150155804A= GRCh38
NC_000005.9:g.149535367A= , CM000667.1:g.149535367A= GRCh37
NC_000005.8:g.149515560A= NCBI36
NG_023367.1:g.5056T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261799.9:c.-414T= MANE Select ENSP00000261799.4:n.-414T=
ENST00000261799.8:c.-414T= ENSP00000261799.4:n.-414T=
ENST00000517660.1:n.57T=
ENST00000520579.5:c.-414T= ENSP00000430026.1:n.-414T=
ENST00000523456.1:n.69T=
NM_002609.3:c.-414T= NP_002600.1:n.-414T=
XM_005268464.2:c.-560T= XP_005268521.1:n.-560T=
XM_011537659.1:c.-881T= XP_011535961.1:n.-881T=
NM_001355016.1:c.-560T= NP_001341945.1:n.-560T=
NM_001355017.1:c.-931T= NP_001341946.1:n.-931T=
NR_149150.1:n.56T=
NM_002609.4:c.-414T= MANE Select NP_002600.1:n.-414T=
NM_001355016.2:c.-560T= NP_001341945.1:n.-560T=
NM_001355017.2:c.-931T= NP_001341946.1:n.-931T=
NR_149150.2:n.42T=