ClinGen Allele Registry
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Canonical Allele Identifier:
CA846003667
Gene: LINC00208
HGNC
NCBI
Linked Data
dbSNP Id:
rs1188508120
gnomAD v3:
8-11577847-G-C
gnomAD v4:
8-11577847-G-C
MyVariant Identifiers:
chr8:g.11435356G>C (hg19)
chr8:g.11577847G>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.11577847G>C , CM000670.2:g.11577847G>C
GRCh38
NC_000008.10:g.11435356G>C , CM000670.1:g.11435356G>C
GRCh37
NC_000008.9:g.11472765G>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_040035.1:n.784-523G>C
Search 100 bp 5'
Search 100 bp 3'