ClinGen Allele Registry
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Canonical Allele Identifier:
CA172383976
Gene: LINC00208
HGNC
NCBI
Linked Data
dbSNP Id:
rs921410473
gnomAD v2:
8-11435454-T-A
gnomAD v3:
8-11577945-T-A
gnomAD v4:
8-11577945-T-A
MyVariant Identifiers:
chr8:g.11435454T>A (hg19)
chr8:g.11577945T>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.11577945T>A , CM000670.2:g.11577945T>A
GRCh38
NC_000008.10:g.11435454T>A , CM000670.1:g.11435454T>A
GRCh37
NC_000008.9:g.11472863T>A
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_040035.1:n.784-425T>A
Search 100 bp 5'
Search 100 bp 3'