Canonical Allele Identifier: CA555909386
Gene: PDGFC HGNC NCBI

Linked Data

dbSNP Id: rs765887781
gnomAD v2: 4-157892947-G-A
gnomAD v3: 4-156971795-G-A
gnomAD v4: 4-156971795-G-A
MyVariant Identifiers: chr4:g.157892947G>A (hg19) chr4:g.156971795G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.156971795G>A , CM000666.2:g.156971795G>A GRCh38
NC_000004.11:g.157892947G>A , CM000666.1:g.157892947G>A GRCh37
NC_000004.10:g.158112397G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502773.6:c.-892C>T MANE Select ENSP00000422464.1:n.-892C>T
NM_016205.3:c.-892C>T MANE Select NP_057289.1:n.-892C>T
NR_036641.2:n.5C>T
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