ClinGen Allele Registry
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Canonical Allele Identifier:
CA15147293
Gene: LINC01768
HGNC
NCBI
Linked Data
dbSNP Id:
rs6537883
gnomAD v2:
1-110405271-T-C
gnomAD v3:
1-109862649-T-C
gnomAD v4:
1-109862649-T-C
MyVariant Identifiers:
chr1:g.110405271T>C (hg19)
chr1:g.109862649T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.109862649T>C , CM000663.2:g.109862649T>C
GRCh38
NC_000001.10:g.110405271T>C , CM000663.1:g.110405271T>C
GRCh37
NC_000001.9:g.110206794T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001738180.2:n.845+29234T>C
Search 100 bp 5'
Search 100 bp 3'