Canonical Allele Identifier: CA1818661832

Gene: PVT1

Linked Data

• dbSNP Id: rs1813856613

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128063410G>A , CM000670.2:g.128063410G>A	GRCh38
NC_000008.10:g.129075656G>A , CM000670.1:g.129075656G>A	GRCh37
NC_000008.9:g.129144838G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_003367.3:n.1213-6750G>A