Canonical Allele Identifier: CA109144501

Gene: PDGFC

Linked Data

• dbSNP Id: rs924185717
• MyVariant Identifiers: chr4:g.157892895C>G (hg19) ; chr4:g.156971743C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.156971743C>G , CM000666.2:g.156971743C>G	GRCh38
NC_000004.11:g.157892895C>G , CM000666.1:g.157892895C>G	GRCh37
NC_000004.10:g.158112345C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502773.6:c.-840G>C MANE Select	ENSP00000422464.1:n.-840G>C
NM_016205.3:c.-840G>C MANE Select	NP_057289.1:n.-840G>C
NR_036641.2:n.57G>C