ClinGen Allele Registry
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Canonical Allele Identifier:
CA1763972892
Gene: LINC00208
HGNC
NCBI
Linked Data
dbSNP Id:
rs1802027400
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.11577932dup , CM000670.2:g.11577932dup
GRCh38
NC_000008.10:g.11435441dup , CM000670.1:g.11435441dup
GRCh37
NC_000008.9:g.11472850dup
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_040035.1:n.784-438dup
Search 100 bp 5'
Search 100 bp 3'