Canonical Allele Identifier: CA185785072
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs1054256846

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127802791G>A , CM000670.2:g.127802791G>A GRCh38
NC_000008.10:g.128815037G>A , CM000670.1:g.128815037G>A GRCh37
NC_000008.9:g.128884219G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.202+8057G>A