Canonical Allele Identifier: CA109144495

Gene: PDGFC

Linked Data

• dbSNP Id: rs980075033
• MyVariant Identifiers: chr4:g.157892884G>C (hg19) ; chr4:g.156971732G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.156971732G>C , CM000666.2:g.156971732G>C	GRCh38
NC_000004.11:g.157892884G>C , CM000666.1:g.157892884G>C	GRCh37
NC_000004.10:g.158112334G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502773.6:c.-829C>G MANE Select	ENSP00000422464.1:n.-829C>G
NM_016205.3:c.-829C>G MANE Select	NP_057289.1:n.-829C>G
NR_036641.2:n.68C>G