Canonical Allele Identifier: CA1818661913
Gene: PVT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063482A= , CM000670.2:g.128063482A= GRCh38
NC_000008.10:g.129075728A= , CM000670.1:g.129075728A= GRCh37
NC_000008.9:g.129144910A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.1213-6678A=