ClinGen Allele Registry
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Canonical Allele Identifier:
CA562420259
Gene: LINC02208
HGNC
NCBI
Linked Data
dbSNP Id:
rs1214400500
gnomAD v2:
5-117701459-A-C
MyVariant Identifiers:
chr5:g.117701459A>C (hg19)
chr5:g.118365764A>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.118365764A>C , CM000667.2:g.118365764A>C
GRCh38
NC_000005.9:g.117701459A>C , CM000667.1:g.117701459A>C
GRCh37
NC_000005.8:g.117729358A>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_104610.1:n.2658-14257T>G
Search 100 bp 5'
Search 100 bp 3'