Canonical Allele Identifier: CA185816183
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs960873209
MyVariant Identifiers: chr8:g.129075658T>C (hg19) chr8:g.128063412T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063412T>C , CM000670.2:g.128063412T>C GRCh38
NC_000008.10:g.129075658T>C , CM000670.1:g.129075658T>C GRCh37
NC_000008.9:g.129144840T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003367.3:n.1213-6748T>C
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