Canonical Allele Identifier: CA1506068250
Gene: PDGFC HGNC NCBI

Linked Data

dbSNP Id: rs1732602295

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.156971797G>A , CM000666.2:g.156971797G>A GRCh38
NC_000004.11:g.157892949G>A , CM000666.1:g.157892949G>A GRCh37
NC_000004.10:g.158112399G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000502773.6:c.-894C>T MANE Select ENSP00000422464.1:n.-894C>T
NM_016205.3:c.-894C>T MANE Select NP_057289.1:n.-894C>T
NR_036641.2:n.3C>T