ClinGen Allele Registry
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Canonical Allele Identifier:
CA846003706
Gene: LINC00208
HGNC
NCBI
Linked Data
dbSNP Id:
rs1163998443
gnomAD v3:
8-11577925-G-T
gnomAD v4:
8-11577925-G-T
MyVariant Identifiers:
chr8:g.11435434G>T (hg19)
chr8:g.11577925G>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.11577925G>T , CM000670.2:g.11577925G>T
GRCh38
NC_000008.10:g.11435434G>T , CM000670.1:g.11435434G>T
GRCh37
NC_000008.9:g.11472843G>T
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_040035.1:n.784-445G>T
Search 100 bp 5'
Search 100 bp 3'