Canonical Allele Identifier: CA1818529788
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs1814479299

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127802730G>T , CM000670.2:g.127802730G>T GRCh38
NC_000008.10:g.128814976G>T , CM000670.1:g.128814976G>T GRCh37
NC_000008.9:g.128884158G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.202+7996G>T