Canonical Allele Identifier: CA1506068145
Gene: PDGFC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.156971691T= , CM000666.2:g.156971691T= GRCh38
NC_000004.11:g.157892843T= , CM000666.1:g.157892843T= GRCh37
NC_000004.10:g.158112293T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502773.6:c.-788A= MANE Select ENSP00000422464.1:n.-788A=
NM_016205.3:c.-788A= MANE Select NP_057289.1:n.-788A=
NR_036641.2:n.109A=
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