Canonical Allele Identifier: CA109144502

Gene: PDGFC

Linked Data

• dbSNP Id: rs924185717
• gnomAD v3: 4-156971743-C-T
• gnomAD v4: 4-156971743-C-T
• MyVariant Identifiers: chr4:g.157892895C>T (hg19) ; chr4:g.156971743C>T (hg38)

Genomic Alleles

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

Transcript Alleles

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