ClinGen Allele Registry
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Canonical Allele Identifier:
CA172383951
Gene: LINC00208
HGNC
NCBI
Linked Data
dbSNP Id:
rs896223685
gnomAD v3:
8-11577810-G-A
gnomAD v4:
8-11577810-G-A
MyVariant Identifiers:
chr8:g.11435319G>A (hg19)
chr8:g.11577810G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.11577810G>A , CM000670.2:g.11577810G>A
GRCh38
NC_000008.10:g.11435319G>A , CM000670.1:g.11435319G>A
GRCh37
NC_000008.9:g.11472728G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_040035.1:n.783+493G>A
Search 100 bp 5'
Search 100 bp 3'