Canonical Allele Identifier: CA1818661849
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs1813856817

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063426T>C , CM000670.2:g.128063426T>C GRCh38
NC_000008.10:g.129075672T>C , CM000670.1:g.129075672T>C GRCh37
NC_000008.9:g.129144854T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.1213-6734T>C