Canonical Allele Identifier: CA1506068241
Gene: PDGFC HGNC NCBI

Linked Data

dbSNP Id: rs765887781

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.156971795G>T , CM000666.2:g.156971795G>T GRCh38
NC_000004.11:g.157892947G>T , CM000666.1:g.157892947G>T GRCh37
NC_000004.10:g.158112397G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000502773.6:c.-892C>A MANE Select ENSP00000422464.1:n.-892C>A
NM_016205.3:c.-892C>A MANE Select NP_057289.1:n.-892C>A
NR_036641.2:n.5C>A