Canonical Allele Identifier: CA185785062

Gene: PVT1

Linked Data

• dbSNP Id: rs973523961
• gnomAD v3: 8-127802741-G-T
• gnomAD v4: 8-127802741-G-T
• MyVariant Identifiers: chr8:g.128814987G>T (hg19) ; chr8:g.127802741G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127802741G>T , CM000670.2:g.127802741G>T	GRCh38
NC_000008.10:g.128814987G>T , CM000670.1:g.128814987G>T	GRCh37
NC_000008.9:g.128884169G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003367.3:n.202+8007G>T