ClinGen Allele Registry
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Canonical Allele Identifier:
CA172383957
Gene: LINC00208
HGNC
NCBI
Linked Data
dbSNP Id:
rs566998144
gnomAD v2:
8-11435357-G-A
gnomAD v3:
8-11577848-G-A
gnomAD v4:
8-11577848-G-A
MyVariant Identifiers:
chr8:g.11435357G>A (hg19)
chr8:g.11577848G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.11577848G>A , CM000670.2:g.11577848G>A
GRCh38
NC_000008.10:g.11435357G>A , CM000670.1:g.11435357G>A
GRCh37
NC_000008.9:g.11472766G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_040035.1:n.784-522G>A
Search 100 bp 5'
Search 100 bp 3'