Canonical Allele Identifier: CA109144496
Gene: PDGFC HGNC NCBI

Linked Data

dbSNP Id: rs567532692
gnomAD v2: 4-157892888-C-T
gnomAD v3: 4-156971736-C-T
gnomAD v4: 4-156971736-C-T
MyVariant Identifiers: chr4:g.157892888C>T (hg19) chr4:g.156971736C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.156971736C>T , CM000666.2:g.156971736C>T GRCh38
NC_000004.11:g.157892888C>T , CM000666.1:g.157892888C>T GRCh37
NC_000004.10:g.158112338C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502773.6:c.-833G>A MANE Select ENSP00000422464.1:n.-833G>A
NM_016205.3:c.-833G>A MANE Select NP_057289.1:n.-833G>A
NR_036641.2:n.64G>A
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Search 100 bp 3'