Canonical Allele Identifier: CA1818661952
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs1813858209

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063513A>G , CM000670.2:g.128063513A>G GRCh38
NC_000008.10:g.129075759A>G , CM000670.1:g.129075759A>G GRCh37
NC_000008.9:g.129144941A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_003367.3:n.1213-6647A>G