Canonical Allele Identifier: CA1818662119
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs2608053

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063586T>A , CM000670.2:g.128063586T>A GRCh38
NC_000008.10:g.129075832T>A , CM000670.1:g.129075832T>A GRCh37
NC_000008.9:g.129145014T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_003367.3:n.1213-6574T>A