ClinGen Allele Registry
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Canonical Allele Identifier:
CA846003752
Gene: LINC00208
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr8:g.11578007T>A
GRCh37
chr8:g.11435516T>A
Linked Data - NCBI & NCI
dbSNP:
10108511
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.11578007T>A , CM000670.2:g.11578007T>A
GRCh38
NC_000008.10:g.11435516T>A , CM000670.1:g.11435516T>A
GRCh37
NC_000008.9:g.11472925T>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_040035.1:n.784-363T>A
Search 100 bp 5'
Search 100 bp 3'