ClinGen Allele Registry
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Canonical Allele Identifier:
CA1763972899
Gene: LINC00208
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.11577937G= , CM000670.2:g.11577937G=
GRCh38
NC_000008.10:g.11435446G= , CM000670.1:g.11435446G=
GRCh37
NC_000008.9:g.11472855G=
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_040035.1:n.784-433G=
Search 100 bp 5'
Search 100 bp 3'