Canonical Allele Identifier: CA789598296
Gene: PDGFC HGNC NCBI

Linked Data

dbSNP Id: rs1255469837
gnomAD v3: 4-156971770-G-T
gnomAD v4: 4-156971770-G-T
MyVariant Identifiers: chr4:g.157892922G>T (hg19) chr4:g.156971770G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.156971770G>T , CM000666.2:g.156971770G>T GRCh38
NC_000004.11:g.157892922G>T , CM000666.1:g.157892922G>T GRCh37
NC_000004.10:g.158112372G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502773.6:c.-867C>A MANE Select ENSP00000422464.1:n.-867C>A
NM_016205.3:c.-867C>A MANE Select NP_057289.1:n.-867C>A
NR_036641.2:n.30C>A
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