Canonical Allele Identifier: CA293666655
Gene: LINC01483 HGNC NCBI

Linked Data

dbSNP Id: rs942247292
gnomAD v3: 17-69854712-AT-A
gnomAD v4: 17-69854712-AT-A
MyVariant Identifiers: chr17:g.67850854del (hg19) chr17:g.69854713del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854715del , CM000679.2:g.69854715del GRCh38
NC_000017.10:g.67850856del , CM000679.1:g.67850856del GRCh37
NC_000017.9:g.65362451del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109971.1:n.363+9229del
NR_109972.1:n.363+9229del
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