Canonical Allele Identifier: CA185816205
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs958355978

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063688G>A , CM000670.2:g.128063688G>A GRCh38
NC_000008.10:g.129075934G>A , CM000670.1:g.129075934G>A GRCh37
NC_000008.9:g.129145116G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.1213-6472G>A