Canonical Allele Identifier: CA555909345
Gene: PDGFC HGNC NCBI

Linked Data

dbSNP Id: rs1462398082
gnomAD v2: 4-157892808-C-T
MyVariant Identifiers: chr4:g.157892808C>T (hg19) chr4:g.156971656C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.156971656C>T , CM000666.2:g.156971656C>T GRCh38
NC_000004.11:g.157892808C>T , CM000666.1:g.157892808C>T GRCh37
NC_000004.10:g.158112258C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502773.6:c.-753G>A MANE Select ENSP00000422464.1:n.-753G>A
NM_016205.3:c.-753G>A MANE Select NP_057289.1:n.-753G>A
NR_036641.2:n.144G>A
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