Canonical Allele Identifier: CA789598257
Gene: PDGFC HGNC NCBI

Linked Data

dbSNP Id: rs962605468
MyVariant Identifiers: chr4:g.157892890_157892891insC (hg19) chr4:g.156971738_156971739insC (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000502773.6:c.-836dup MANE Select ENSP00000422464.1:n.-836dup
NM_016205.3:c.-836dup MANE Select NP_057289.1:n.-836dup
NR_036641.2:n.61dup
Search 100 bp 5'
Search 100 bp 3'