Canonical Allele Identifier: CA1818661900
Gene: PVT1 HGNC NCBI

Linked Data

dbSNP Id: rs1813857375
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128063467G>A , CM000670.2:g.128063467G>A GRCh38
NC_000008.10:g.129075713G>A , CM000670.1:g.129075713G>A GRCh37
NC_000008.9:g.129144895G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_003367.3:n.1213-6693G>A
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Search 100 bp 3'