Canonical Allele Identifier: CA2675965115
Gene: PDGFRB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150120846_150120851del , CM000667.2:g.150120846_150120851del GRCh38
NC_000005.9:g.149500409_149500414del , CM000667.1:g.149500409_149500414del GRCh37
NC_000005.8:g.149480602_149480607del NCBI36
NG_023367.1:g.40012_40017del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261799.9:c.2586+40_2586+45del MANE Select ENSP00000261799.4:n.2586+40_2586+45del
ENST00000261799.8:c.2586+40_2586+45del ENSP00000261799.4:n.2586+40_2586+45del
ENST00000519575.5:n.500+40_500+45del
ENST00000520579.5:c.*1900+40_*1900+45del ENSP00000430026.1:n.*1900+40_*1900+45del
NM_002609.3:c.2586+40_2586+45del NP_002600.1:n.2586+40_2586+45del
XM_005268464.2:c.2394+40_2394+45del XP_005268521.1:n.2394+40_2394+45del
XM_011537658.1:c.2586+40_2586+45del XP_011535960.1:n.2586+40_2586+45del
XM_011537659.1:c.2586+40_2586+45del XP_011535961.1:n.2586+40_2586+45del
XM_011537660.1:c.2586+40_2586+45del XP_011535962.1:n.2586+40_2586+45del
NM_001355016.1:c.2394+40_2394+45del NP_001341945.1:n.2394+40_2394+45del
NM_001355017.1:c.2103+40_2103+45del NP_001341946.1:n.2103+40_2103+45del
NM_002609.4:c.2586+40_2586+45del MANE Select NP_002600.1:n.2586+40_2586+45del
NM_001355016.2:c.2394+40_2394+45del NP_001341945.1:n.2394+40_2394+45del
NM_001355017.2:c.2103+40_2103+45del NP_001341946.1:n.2103+40_2103+45del