Canonical Allele Identifier: CA1818662239
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs1813861118

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063660A>C , CM000670.2:g.128063660A>C GRCh38
NC_000008.10:g.129075906A>C , CM000670.1:g.129075906A>C GRCh37
NC_000008.9:g.129145088A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_003367.3:n.1213-6500A>C