Canonical Allele Identifier: CA1119063674

Gene: PVT1

Linked Data

• dbSNP Id: rs1813857644
• gnomAD v3: 8-128063480-CCA-C
• gnomAD v4: 8-128063480-CCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128063481_128063482del , CM000670.2:g.128063481_128063482del	GRCh38
NC_000008.10:g.129075727_129075728del , CM000670.1:g.129075727_129075728del	GRCh37
NC_000008.9:g.129144909_129144910del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003367.3:n.1213-6679_1213-6678del