Canonical Allele Identifier: CA1818661956
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs1332480928

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063527_128063530del , CM000670.2:g.128063527_128063530del GRCh38
NC_000008.10:g.129075773_129075776del , CM000670.1:g.129075773_129075776del GRCh37
NC_000008.9:g.129144955_129144958del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_003367.3:n.1213-6633_1213-6630del