Canonical Allele Identifier: CA585097043
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs1303704620

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063687A>T , CM000670.2:g.128063687A>T GRCh38
NC_000008.10:g.129075933A>T , CM000670.1:g.129075933A>T GRCh37
NC_000008.9:g.129145115A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.1213-6473A>T