Canonical Allele Identifier: CA1590817254
Gene: PDGFRB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150155824C= , CM000667.2:g.150155824C= GRCh38
NC_000005.9:g.149535387C= , CM000667.1:g.149535387C= GRCh37
NC_000005.8:g.149515580C= NCBI36
NG_023367.1:g.5036G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261799.9:c.-434G= MANE Select ENSP00000261799.4:n.-434G=
ENST00000261799.8:c.-434G= ENSP00000261799.4:n.-434G=
ENST00000517660.1:n.37G=
ENST00000520579.5:c.-434G= ENSP00000430026.1:n.-434G=
ENST00000523456.1:n.49G=
NM_002609.3:c.-434G= NP_002600.1:n.-434G=
XM_005268464.2:c.-580G= XP_005268521.1:n.-580G=
XM_011537659.1:c.-901G= XP_011535961.1:n.-901G=
NM_001355016.1:c.-580G= NP_001341945.1:n.-580G=
NM_001355017.1:c.-951G= NP_001341946.1:n.-951G=
NR_149150.1:n.36G=
NM_002609.4:c.-434G= MANE Select NP_002600.1:n.-434G=
NM_001355016.2:c.-580G= NP_001341945.1:n.-580G=
NM_001355017.2:c.-951G= NP_001341946.1:n.-951G=
NR_149150.2:n.22G=