Canonical Allele Identifier: CA1818662046
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs1813859018

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063553G>C , CM000670.2:g.128063553G>C GRCh38
NC_000008.10:g.129075799G>C , CM000670.1:g.129075799G>C GRCh37
NC_000008.9:g.129144981G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.1213-6607G>C