Canonical Allele Identifier: CA1119063745

Gene: PVT1

Linked Data

• dbSNP Id: rs1813860980
• gnomAD v3: 8-128063648-G-A
• gnomAD v4: 8-128063648-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128063648G>A , CM000670.2:g.128063648G>A	GRCh38
NC_000008.10:g.129075894G>A , CM000670.1:g.129075894G>A	GRCh37
NC_000008.9:g.129145076G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_003367.3:n.1213-6512G>A