Canonical Allele Identifier: CA109144497
Gene: PDGFC HGNC NCBI

Linked Data

dbSNP Id: rs962605468

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.156971744del , CM000666.2:g.156971744del GRCh38
NC_000004.11:g.157892896del , CM000666.1:g.157892896del GRCh37
NC_000004.10:g.158112346del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502773.6:c.-836del MANE Select ENSP00000422464.1:n.-836del
NM_016205.3:c.-836del MANE Select NP_057289.1:n.-836del
NR_036641.2:n.61del