Canonical Allele Identifier: CA1818529927
Gene: PVT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127802820T= , CM000670.2:g.127802820T= GRCh38
NC_000008.10:g.128815066T= , CM000670.1:g.128815066T= GRCh37
NC_000008.9:g.128884248T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.202+8086T=