Canonical Allele Identifier: CA555902789

Gene: PDGFC

Linked Data

• dbSNP Id: rs1463623237
• gnomAD v2: 4-157683599-C-T
• gnomAD v3: 4-156762447-C-T
• gnomAD v4: 4-156762447-C-T
• MyVariant Identifiers: chr4:g.157683599C>T (hg19) ; chr4:g.156762447C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.156762447C>T , CM000666.2:g.156762447C>T	GRCh38
NC_000004.11:g.157683599C>T , CM000666.1:g.157683599C>T	GRCh37
NC_000004.10:g.157903049C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000502773.6:c.*643G>A MANE Select	ENSP00000422464.1:n.*643G>A
ENST00000274071.6:c.*1589G>A	ENSP00000274071.2:n.*1589G>A
ENST00000502773.5:c.*643G>A	ENSP00000422464.1:n.*643G>A
NM_016205.2:c.*643G>A	NP_057289.1:n.*643G>A
NR_036641.1:n.2233G>A
XM_011532124.1:c.*643G>A	XP_011530426.1:n.*643G>A
XM_011532125.1:c.*643G>A	XP_011530427.1:n.*643G>A
XM_011532124.2:c.*643G>A	XP_011530426.1:n.*643G>A
XM_017008455.1:c.*643G>A	XP_016863944.1:n.*643G>A
XM_017008456.2:c.*643G>A	XP_016863945.1:n.*643G>A
NM_016205.3:c.*643G>A MANE Select	NP_057289.1:n.*643G>A
NR_036641.2:n.2638G>A