Canonical Allele Identifier: CA1818529793
Gene: PVT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127802739A= , CM000670.2:g.127802739A= GRCh38
NC_000008.10:g.128814985A= , CM000670.1:g.128814985A= GRCh37
NC_000008.9:g.128884167A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.202+8005A=