Canonical Allele Identifier: CA847236544

Gene: PVT1 MIR1206

Linked Data

• dbSNP Id: rs2114358
• gnomAD v4: 8-128008933-G-C
• MyVariant Identifiers: chr8:g.129021179G>C (hg19) ; chr8:g.128008933G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128008933G>C , CM000670.2:g.128008933G>C	GRCh38
NC_000008.10:g.129021179G>C , CM000670.1:g.129021179G>C	GRCh37
NC_000008.9:g.129090361G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_003367.3:n.1212+19642G>C (PVT1)
NR_031611.1:n.36G>C (MIR1206)