Canonical Allele Identifier: CA293666652
Gene: LINC01483 HGNC NCBI

Linked Data

dbSNP Id: rs898350286
gnomAD v2: 17-67850837-T-A
gnomAD v3: 17-69854696-T-A
gnomAD v4: 17-69854696-T-A
MyVariant Identifiers: chr17:g.67850837T>A (hg19) chr17:g.69854696T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854696T>A , CM000679.2:g.69854696T>A GRCh38
NC_000017.10:g.67850837T>A , CM000679.1:g.67850837T>A GRCh37
NC_000017.9:g.65362432T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109971.1:n.363+9210T>A
NR_109972.1:n.363+9210T>A
Search 100 bp 5'
Search 100 bp 3'