ClinGen Allele Registry
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Canonical Allele Identifier:
CA847293997
Gene: LINC00824
HGNC
NCBI
Linked Data
dbSNP Id:
rs1165448235
gnomAD v3:
8-128529891-A-C
gnomAD v4:
8-128529891-A-C
MyVariant Identifiers:
chr8:g.129542137A>C (hg19)
chr8:g.128529891A>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.128529891A>C , CM000670.2:g.128529891A>C
GRCh38
NC_000008.10:g.129542137A>C , CM000670.1:g.129542137A>C
GRCh37
NC_000008.9:g.129611319A>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_121672.1:n.508+31179T>G
Search 100 bp 5'
Search 100 bp 3'