Canonical Allele Identifier: CA2768885168
Gene: PDGFRB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150155774_150155775insGGTGGTCG , CM000667.2:g.150155774_150155775insGGTGGTCG GRCh38
NC_000005.9:g.149535337_149535338insGGTGGTCG , CM000667.1:g.149535337_149535338insGGTGGTCG GRCh37
NC_000005.8:g.149515530_149515531insGGTGGTCG NCBI36
NG_023367.1:g.5085_5086insCGACCACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261799.9:c.-385_-384insCGACCACC MANE Select ENSP00000261799.4:n.-385_-384insCGACCACC
ENST00000261799.8:c.-385_-384insCGACCACC ENSP00000261799.4:n.-385_-384insCGACCACC
ENST00000517660.1:n.86_87insCGACCACC
ENST00000520579.5:c.-385_-384insCGACCACC ENSP00000430026.1:n.-385_-384insCGACCACC
ENST00000523456.1:n.98_99insCGACCACC
NM_002609.3:c.-385_-384insCGACCACC NP_002600.1:n.-385_-384insCGACCACC
XM_005268464.2:c.-531_-530insCGACCACC XP_005268521.1:n.-531_-530insCGACCACC
XM_011537659.1:c.-852_-851insCGACCACC XP_011535961.1:n.-852_-851insCGACCACC
NM_001355016.1:c.-531_-530insCGACCACC NP_001341945.1:n.-531_-530insCGACCACC
NM_001355017.1:c.-902_-901insCGACCACC NP_001341946.1:n.-902_-901insCGACCACC
NR_149150.1:n.85_86insCGACCACC
NM_002609.4:c.-385_-384insCGACCACC MANE Select NP_002600.1:n.-385_-384insCGACCACC
NM_001355016.2:c.-531_-530insCGACCACC NP_001341945.1:n.-531_-530insCGACCACC
NM_001355017.2:c.-902_-901insCGACCACC NP_001341946.1:n.-902_-901insCGACCACC
NR_149150.2:n.71_72insCGACCACC