Canonical Allele Identifier: CA1590817251
Gene: PDGFRB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150155817G= , CM000667.2:g.150155817G= GRCh38
NC_000005.9:g.149535380G= , CM000667.1:g.149535380G= GRCh37
NC_000005.8:g.149515573G= NCBI36
NG_023367.1:g.5043C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261799.9:c.-427C= MANE Select ENSP00000261799.4:n.-427C=
ENST00000261799.8:c.-427C= ENSP00000261799.4:n.-427C=
ENST00000517660.1:n.44C=
ENST00000520579.5:c.-427C= ENSP00000430026.1:n.-427C=
ENST00000523456.1:n.56C=
NM_002609.3:c.-427C= NP_002600.1:n.-427C=
XM_005268464.2:c.-573C= XP_005268521.1:n.-573C=
XM_011537659.1:c.-894C= XP_011535961.1:n.-894C=
NM_001355016.1:c.-573C= NP_001341945.1:n.-573C=
NM_001355017.1:c.-944C= NP_001341946.1:n.-944C=
NR_149150.1:n.43C=
NM_002609.4:c.-427C= MANE Select NP_002600.1:n.-427C=
NM_001355016.2:c.-573C= NP_001341945.1:n.-573C=
NM_001355017.2:c.-944C= NP_001341946.1:n.-944C=
NR_149150.2:n.29C=