ClinGen Allele Registry
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Canonical Allele Identifier:
CA1818529786
Gene: PVT1
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.127802730G= , CM000670.2:g.127802730G=
GRCh38
NC_000008.10:g.128814976G= , CM000670.1:g.128814976G=
GRCh37
NC_000008.9:g.128884158G=
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_003367.3:n.202+7996G=
Search 100 bp 5'
Search 100 bp 3'