Canonical Allele Identifier: CA1818661942
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs1813858150

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063503C>T , CM000670.2:g.128063503C>T GRCh38
NC_000008.10:g.129075749C>T , CM000670.1:g.129075749C>T GRCh37
NC_000008.9:g.129144931C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_003367.3:n.1213-6657C>T