Canonical Allele Identifier: CA1119039368
Gene: PVT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127802789del , CM000670.2:g.127802789del GRCh38
NC_000008.10:g.128815035del , CM000670.1:g.128815035del GRCh37
NC_000008.9:g.128884217del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.202+8055del