Canonical Allele Identifier: CA185785077
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs550838210

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127802817A>C , CM000670.2:g.127802817A>C GRCh38
NC_000008.10:g.128815063A>C , CM000670.1:g.128815063A>C GRCh37
NC_000008.9:g.128884245A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.202+8083A>C