Canonical Allele Identifier: CA2782153610
Gene: PVT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063515A>G , CM000670.2:g.128063515A>G GRCh38
NC_000008.10:g.129075761A>G , CM000670.1:g.129075761A>G GRCh37
NC_000008.9:g.129144943A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_003367.3:n.1213-6645A>G