Canonical Allele Identifier: CA185816197

Gene: PVT1

Linked Data

• dbSNP Id: rs1009727095
• gnomAD v3: 8-128063569-C-T
• gnomAD v4: 8-128063569-C-T
• MyVariant Identifiers: chr8:g.129075815C>T (hg19) ; chr8:g.128063569C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128063569C>T , CM000670.2:g.128063569C>T	GRCh38
NC_000008.10:g.129075815C>T , CM000670.1:g.129075815C>T	GRCh37
NC_000008.9:g.129144997C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003367.3:n.1213-6591C>T