Canonical Allele Identifier: CA1818662237
Gene: PVT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063660A= , CM000670.2:g.128063660A= GRCh38
NC_000008.10:g.129075906A= , CM000670.1:g.129075906A= GRCh37
NC_000008.9:g.129145088A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_003367.3:n.1213-6500A=