Canonical Allele Identifier: CA293666673
Gene: LINC01483 HGNC NCBI

Linked Data

dbSNP Id: rs190700385
gnomAD v3: 17-69854851-G-T
gnomAD v4: 17-69854851-G-T
MyVariant Identifiers: chr17:g.67850992G>T (hg19) chr17:g.69854851G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854851G>T , CM000679.2:g.69854851G>T GRCh38
NC_000017.10:g.67850992G>T , CM000679.1:g.67850992G>T GRCh37
NC_000017.9:g.65362587G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109971.1:n.363+9365G>T
NR_109972.1:n.363+9365G>T
Search 100 bp 5'
Search 100 bp 3'