Canonical Allele Identifier: CA847233490

Gene: PVT1

Linked Data

• dbSNP Id: rs1169824958
• MyVariant Identifiers: chr8:g.129075659_129075660del (hg19) ; chr8:g.128063413_128063414del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128063415_128063416del , CM000670.2:g.128063415_128063416del	GRCh38
NC_000008.10:g.129075661_129075662del , CM000670.1:g.129075661_129075662del	GRCh37
NC_000008.9:g.129144843_129144844del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003367.3:n.1213-6745_1213-6744del