Canonical Allele Identifier: CA2718185604
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs2129645223

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127802742T>G , CM000670.2:g.127802742T>G GRCh38
NC_000008.10:g.128814988T>G , CM000670.1:g.128814988T>G GRCh37
NC_000008.9:g.128884170T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.202+8008T>G