ClinGen Allele Registry
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Canonical Allele Identifier:
CA903927127
Gene: LINC02043
HGNC
NCBI
Linked Data
dbSNP Id:
rs1293003165
gnomAD v3:
3-186812658-A-T
gnomAD v4:
3-186812658-A-T
MyVariant Identifiers:
chr3:g.186530447A>T (hg19)
chr3:g.186812658A>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.186812658A>T , CM000665.2:g.186812658A>T
GRCh38
NC_000003.11:g.186530447A>T , CM000665.1:g.186530447A>T
GRCh37
NC_000003.10:g.188013141A>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_125409.1:n.564-510T>A
Search 100 bp 5'
Search 100 bp 3'