Canonical Allele Identifier: CA2782153614
Gene: PVT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063550C>T , CM000670.2:g.128063550C>T GRCh38
NC_000008.10:g.129075796C>T , CM000670.1:g.129075796C>T GRCh37
NC_000008.9:g.129144978C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.1213-6610C>T