Canonical Allele Identifier: CA1818656869
Gene: PVT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128059915G>T , CM000670.2:g.128059915G>T GRCh38
NC_000008.10:g.129072161G>T , CM000670.1:g.129072161G>T GRCh37
NC_000008.9:g.129141343G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.1213-10245G>T