Canonical Allele Identifier: CA1505969302
Gene: PDGFC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.156762471C= , CM000666.2:g.156762471C= GRCh38
NC_000004.11:g.157683623C= , CM000666.1:g.157683623C= GRCh37
NC_000004.10:g.157903073C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502773.6:c.*619G= MANE Select ENSP00000422464.1:n.*619G=
ENST00000274071.6:c.*1565G= ENSP00000274071.2:n.*1565G=
ENST00000502773.5:c.*619G= ENSP00000422464.1:n.*619G=
NM_016205.2:c.*619G= NP_057289.1:n.*619G=
NR_036641.1:n.2209G=
XM_011532124.1:c.*619G= XP_011530426.1:n.*619G=
XM_011532125.1:c.*619G= XP_011530427.1:n.*619G=
XM_011532124.2:c.*619G= XP_011530426.1:n.*619G=
XM_017008455.1:c.*619G= XP_016863944.1:n.*619G=
XM_017008456.2:c.*619G= XP_016863945.1:n.*619G=
NM_016205.3:c.*619G= MANE Select NP_057289.1:n.*619G=
NR_036641.2:n.2614G=