Canonical Allele Identifier: CA185816190

Gene: PVT1

Linked Data

• dbSNP Id: rs755160448
• gnomAD v3: 8-128063481-C-T
• gnomAD v4: 8-128063481-C-T
• MyVariant Identifiers: chr8:g.129075727C>T (hg19) ; chr8:g.128063481C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128063481C>T , CM000670.2:g.128063481C>T	GRCh38
NC_000008.10:g.129075727C>T , CM000670.1:g.129075727C>T	GRCh37
NC_000008.9:g.129144909C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003367.3:n.1213-6679C>T