Canonical Allele Identifier: CA1590817246
Gene: PDGFRB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150155802C= , CM000667.2:g.150155802C= GRCh38
NC_000005.9:g.149535365C= , CM000667.1:g.149535365C= GRCh37
NC_000005.8:g.149515558C= NCBI36
NG_023367.1:g.5058G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261799.9:c.-412G= MANE Select ENSP00000261799.4:n.-412G=
ENST00000261799.8:c.-412G= ENSP00000261799.4:n.-412G=
ENST00000517660.1:n.59G=
ENST00000520579.5:c.-412G= ENSP00000430026.1:n.-412G=
ENST00000523456.1:n.71G=
NM_002609.3:c.-412G= NP_002600.1:n.-412G=
XM_005268464.2:c.-558G= XP_005268521.1:n.-558G=
XM_011537659.1:c.-879G= XP_011535961.1:n.-879G=
NM_001355016.1:c.-558G= NP_001341945.1:n.-558G=
NM_001355017.1:c.-929G= NP_001341946.1:n.-929G=
NR_149150.1:n.58G=
NM_002609.4:c.-412G= MANE Select NP_002600.1:n.-412G=
NM_001355016.2:c.-558G= NP_001341945.1:n.-558G=
NM_001355017.2:c.-929G= NP_001341946.1:n.-929G=
NR_149150.2:n.44G=