Canonical Allele Identifier: CA847233555
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs150359865
gnomAD v3: 8-128063553-GACAC-G
gnomAD v4: 8-128063553-GACAC-G
MyVariant Identifiers: chr8:g.129075800_129075803del (hg19) chr8:g.128063554_128063557del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063567_128063570del , CM000670.2:g.128063567_128063570del GRCh38
NC_000008.10:g.129075813_129075816del , CM000670.1:g.129075813_129075816del GRCh37
NC_000008.9:g.129144995_129144998del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.1213-6593_1213-6590del
Search 100 bp 5'
Search 100 bp 3'