Canonical Allele Identifier: CA1590817237
Gene: PDGFRB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150155773T= , CM000667.2:g.150155773T= GRCh38
NC_000005.9:g.149535336T= , CM000667.1:g.149535336T= GRCh37
NC_000005.8:g.149515529T= NCBI36
NG_023367.1:g.5087A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261799.9:c.-383A= MANE Select ENSP00000261799.4:n.-383A=
ENST00000261799.8:c.-383A= ENSP00000261799.4:n.-383A=
ENST00000517660.1:n.88A=
ENST00000520579.5:c.-383A= ENSP00000430026.1:n.-383A=
ENST00000523456.1:n.100A=
NM_002609.3:c.-383A= NP_002600.1:n.-383A=
XM_005268464.2:c.-529A= XP_005268521.1:n.-529A=
XM_011537659.1:c.-850A= XP_011535961.1:n.-850A=
NM_001355016.1:c.-529A= NP_001341945.1:n.-529A=
NM_001355017.1:c.-900A= NP_001341946.1:n.-900A=
NR_149150.1:n.87A=
NM_002609.4:c.-383A= MANE Select NP_002600.1:n.-383A=
NM_001355016.2:c.-529A= NP_001341945.1:n.-529A=
NM_001355017.2:c.-900A= NP_001341946.1:n.-900A=
NR_149150.2:n.73A=