Canonical Allele Identifier: CA789598252

Gene: PDGFC

Linked Data

• dbSNP Id: rs1347678087
• gnomAD v3: 4-156971738-T-C
• gnomAD v4: 4-156971738-T-C
• MyVariant Identifiers: chr4:g.157892890T>C (hg19) ; chr4:g.156971738T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.156971738T>C , CM000666.2:g.156971738T>C	GRCh38
NC_000004.11:g.157892890T>C , CM000666.1:g.157892890T>C	GRCh37
NC_000004.10:g.158112340T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502773.6:c.-835A>G MANE Select	ENSP00000422464.1:n.-835A>G
NM_016205.3:c.-835A>G MANE Select	NP_057289.1:n.-835A>G
NR_036641.2:n.62A>G