ClinGen Allele Registry
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Canonical Allele Identifier:
CA172383952
Gene: LINC00208
HGNC
NCBI
Linked Data
dbSNP Id:
rs577436916
gnomAD v3:
8-11577812-C-T
gnomAD v4:
8-11577812-C-T
MyVariant Identifiers:
chr8:g.11435321C>T (hg19)
chr8:g.11577812C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.11577812C>T , CM000670.2:g.11577812C>T
GRCh38
NC_000008.10:g.11435321C>T , CM000670.1:g.11435321C>T
GRCh37
NC_000008.9:g.11472730C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_040035.1:n.783+495C>T
Search 100 bp 5'
Search 100 bp 3'