Canonical Allele Identifier: CA1818661861

Gene: PVT1

Linked Data

• dbSNP Id: rs921356948

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128063436C>A , CM000670.2:g.128063436C>A	GRCh38
NC_000008.10:g.129075682C>A , CM000670.1:g.129075682C>A	GRCh37
NC_000008.9:g.129144864C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_003367.3:n.1213-6724C>A