ClinGen Allele Registry
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Canonical Allele Identifier:
CA89646406
Gene: LINC02043
HGNC
NCBI
Linked Data
dbSNP Id:
rs527965616
gnomAD v2:
3-186530461-C-T
gnomAD v3:
3-186812672-C-T
gnomAD v4:
3-186812672-C-T
MyVariant Identifiers:
chr3:g.186530461C>T (hg19)
chr3:g.186812672C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.186812672C>T , CM000665.2:g.186812672C>T
GRCh38
NC_000003.11:g.186530461C>T , CM000665.1:g.186530461C>T
GRCh37
NC_000003.10:g.188013155C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_125409.1:n.564-524G>A
Search 100 bp 5'
Search 100 bp 3'