Canonical Allele Identifier: CA1119063708
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs1813858913
gnomAD v3: 8-128063547-G-A
gnomAD v4: 8-128063547-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063547G>A , CM000670.2:g.128063547G>A GRCh38
NC_000008.10:g.129075793G>A , CM000670.1:g.129075793G>A GRCh37
NC_000008.9:g.129144975G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.1213-6613G>A
Search 100 bp 5'
Search 100 bp 3'