Canonical Allele Identifier: CA1818529901
Gene: PVT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127802803C= , CM000670.2:g.127802803C= GRCh38
NC_000008.10:g.128815049C= , CM000670.1:g.128815049C= GRCh37
NC_000008.9:g.128884231C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.202+8069C=