Canonical Allele Identifier: CA789566878

Gene: PDGFC

Linked Data

• dbSNP Id: rs1424019776
• gnomAD v3: 4-156762456-C-A
• gnomAD v4: 4-156762456-C-A
• MyVariant Identifiers: chr4:g.157683608C>A (hg19) ; chr4:g.156762456C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.156762456C>A , CM000666.2:g.156762456C>A	GRCh38
NC_000004.11:g.157683608C>A , CM000666.1:g.157683608C>A	GRCh37
NC_000004.10:g.157903058C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502773.6:c.*634G>T MANE Select	ENSP00000422464.1:n.*634G>T
ENST00000274071.6:c.*1580G>T	ENSP00000274071.2:n.*1580G>T
ENST00000502773.5:c.*634G>T	ENSP00000422464.1:n.*634G>T
NM_016205.2:c.*634G>T	NP_057289.1:n.*634G>T
NR_036641.1:n.2224G>T
XM_011532124.1:c.*634G>T	XP_011530426.1:n.*634G>T
XM_011532125.1:c.*634G>T	XP_011530427.1:n.*634G>T
XM_011532124.2:c.*634G>T	XP_011530426.1:n.*634G>T
XM_017008455.1:c.*634G>T	XP_016863944.1:n.*634G>T
XM_017008456.2:c.*634G>T	XP_016863945.1:n.*634G>T
NM_016205.3:c.*634G>T MANE Select	NP_057289.1:n.*634G>T
NR_036641.2:n.2629G>T