Canonical Allele Identifier: CA15552757
Gene: PVT1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2608053

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063586T>C , CM000670.2:g.128063586T>C GRCh38
NC_000008.10:g.129075832T>C , CM000670.1:g.129075832T>C GRCh37
NC_000008.9:g.129145014T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_003367.3:n.1213-6574T>C