Canonical Allele Identifier: CA2768885174
Gene: PDGFRB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150155827del , CM000667.2:g.150155827del GRCh38
NC_000005.9:g.149535390del , CM000667.1:g.149535390del GRCh37
NC_000005.8:g.149515583del NCBI36
NG_023367.1:g.5035del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261799.9:c.-435del MANE Select ENSP00000261799.4:n.-435del
ENST00000261799.8:c.-435del ENSP00000261799.4:n.-435del
ENST00000517660.1:n.36del
ENST00000520579.5:c.-435del ENSP00000430026.1:n.-435del
ENST00000523456.1:n.48del
NM_002609.3:c.-435del NP_002600.1:n.-435del
XM_005268464.2:c.-581del XP_005268521.1:n.-581del
XM_011537659.1:c.-902del XP_011535961.1:n.-902del
NM_001355016.1:c.-581del NP_001341945.1:n.-581del
NM_001355017.1:c.-952del NP_001341946.1:n.-952del
NR_149150.1:n.35del
NM_002609.4:c.-435del MANE Select NP_002600.1:n.-435del
NM_001355016.2:c.-581del NP_001341945.1:n.-581del
NM_001355017.2:c.-952del NP_001341946.1:n.-952del
NR_149150.2:n.21del