Canonical Allele Identifier: CA1069887507
Gene: PDGFC HGNC NCBI

Linked Data

dbSNP Id: rs1732601502
gnomAD v3: 4-156971772-G-A
gnomAD v4: 4-156971772-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.156971772G>A , CM000666.2:g.156971772G>A GRCh38
NC_000004.11:g.157892924G>A , CM000666.1:g.157892924G>A GRCh37
NC_000004.10:g.158112374G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502773.6:c.-869C>T MANE Select ENSP00000422464.1:n.-869C>T
NM_016205.3:c.-869C>T MANE Select NP_057289.1:n.-869C>T
NR_036641.2:n.28C>T
Search 100 bp 5'
Search 100 bp 3'