Canonical Allele Identifier: CA1818662099
Gene: PVT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063580A= , CM000670.2:g.128063580A= GRCh38
NC_000008.10:g.129075826A= , CM000670.1:g.129075826A= GRCh37
NC_000008.9:g.129145008A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.1213-6580A=