Canonical Allele Identifier: CA2675965065
Gene: PDGFRB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150120832_150120833del , CM000667.2:g.150120832_150120833del GRCh38
NC_000005.9:g.149500395_149500396del , CM000667.1:g.149500395_149500396del GRCh37
NC_000005.8:g.149480588_149480589del NCBI36
NG_023367.1:g.40028_40029del

Transcript Alleles

HGVS Amino-acid change
ENST00000261799.9:c.2586+56_2586+57del MANE Select ENSP00000261799.4:n.2586+56_2586+57del
ENST00000261799.8:c.2586+56_2586+57del ENSP00000261799.4:n.2586+56_2586+57del
ENST00000519575.5:n.500+56_500+57del
ENST00000520579.5:c.*1900+56_*1900+57del ENSP00000430026.1:n.*1900+56_*1900+57del
NM_002609.3:c.2586+56_2586+57del NP_002600.1:n.2586+56_2586+57del
XM_005268464.2:c.2394+56_2394+57del XP_005268521.1:n.2394+56_2394+57del
XM_011537658.1:c.2586+56_2586+57del XP_011535960.1:n.2586+56_2586+57del
XM_011537659.1:c.2586+56_2586+57del XP_011535961.1:n.2586+56_2586+57del
XM_011537660.1:c.2586+56_2586+57del XP_011535962.1:n.2586+56_2586+57del
NM_001355016.1:c.2394+56_2394+57del NP_001341945.1:n.2394+56_2394+57del
NM_001355017.1:c.2103+56_2103+57del NP_001341946.1:n.2103+56_2103+57del
NM_002609.4:c.2586+56_2586+57del MANE Select NP_002600.1:n.2586+56_2586+57del
NM_001355016.2:c.2394+56_2394+57del NP_001341945.1:n.2394+56_2394+57del
NM_001355017.2:c.2103+56_2103+57del NP_001341946.1:n.2103+56_2103+57del