Canonical Allele Identifier: CA789598245

Gene: PDGFC

Linked Data

• dbSNP Id: rs1241809184
• gnomAD v3: 4-156971721-G-A
• gnomAD v4: 4-156971721-G-A
• MyVariant Identifiers: chr4:g.157892873G>A (hg19) ; chr4:g.156971721G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.156971721G>A , CM000666.2:g.156971721G>A	GRCh38
NC_000004.11:g.157892873G>A , CM000666.1:g.157892873G>A	GRCh37
NC_000004.10:g.158112323G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502773.6:c.-818C>T MANE Select	ENSP00000422464.1:n.-818C>T
NM_016205.3:c.-818C>T MANE Select	NP_057289.1:n.-818C>T
NR_036641.2:n.79C>T