Canonical Allele Identifier: CA2782153612
Gene: PVT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063536G>T , CM000670.2:g.128063536G>T GRCh38
NC_000008.10:g.129075782G>T , CM000670.1:g.129075782G>T GRCh37
NC_000008.9:g.129144964G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.1213-6624G>T