Canonical Allele Identifier: CA109120387

Gene: PDGFC

Linked Data

• dbSNP Id: rs770167106
• gnomAD v2: 4-157683703-T-C
• gnomAD v3: 4-156762551-T-C
• gnomAD v4: 4-156762551-T-C
• MyVariant Identifiers: chr4:g.157683703T>C (hg19) ; chr4:g.156762551T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.156762551T>C , CM000666.2:g.156762551T>C	GRCh38
NC_000004.11:g.157683703T>C , CM000666.1:g.157683703T>C	GRCh37
NC_000004.10:g.157903153T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000502773.6:c.*539A>G MANE Select	ENSP00000422464.1:n.*539A>G
ENST00000274071.6:c.*1485A>G	ENSP00000274071.2:n.*1485A>G
ENST00000502773.5:c.*539A>G	ENSP00000422464.1:n.*539A>G
NM_016205.2:c.*539A>G	NP_057289.1:n.*539A>G
NR_036641.1:n.2129A>G
XM_011532124.1:c.*539A>G	XP_011530426.1:n.*539A>G
XM_011532125.1:c.*539A>G	XP_011530427.1:n.*539A>G
XM_011532124.2:c.*539A>G	XP_011530426.1:n.*539A>G
XM_017008455.1:c.*539A>G	XP_016863944.1:n.*539A>G
XM_017008456.2:c.*539A>G	XP_016863945.1:n.*539A>G
NM_016205.3:c.*539A>G MANE Select	NP_057289.1:n.*539A>G
NR_036641.2:n.2534A>G