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Canonical Allele Identifier:
CA15552757
Gene: PVT1
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr8:g.128063586T>C
GRCh37
chr8:g.129075832T>C
Linked Data - Sequence & Population
gnomAD v2:
8:129075832 T / C
gnomAD v3:
8:128063586 T / C
gnomAD v4:
chr8-128063586-T-C
Joint Max Group AF
0.72104208 (EAS)
Genomes Max Group AF
0.72104208 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2608053
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.128063586T>C , CM000670.2:g.128063586T>C
GRCh38
NC_000008.10:g.129075832T>C , CM000670.1:g.129075832T>C
GRCh37
NC_000008.9:g.129145014T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_003367.3:n.1213-6574T>C
Search 100 bp 5'
Search 100 bp 3'