Canonical Allele Identifier: CA1818529865
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs4410871

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127802783T>A , CM000670.2:g.127802783T>A GRCh38
NC_000008.10:g.128815029T>A , CM000670.1:g.128815029T>A GRCh37
NC_000008.9:g.128884211T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_003367.3:n.202+8049T>A