ClinGen Allele Registry
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Canonical Allele Identifier:
CA585119933
Gene: LINC00824
HGNC
NCBI
Linked Data
dbSNP Id:
rs1314153962
gnomAD v2:
8-129542418-C-T
gnomAD v3:
8-128530172-C-T
gnomAD v4:
8-128530172-C-T
MyVariant Identifiers:
chr8:g.129542418C>T (hg19)
chr8:g.128530172C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.128530172C>T , CM000670.2:g.128530172C>T
GRCh38
NC_000008.10:g.129542418C>T , CM000670.1:g.129542418C>T
GRCh37
NC_000008.9:g.129611600C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_121672.1:n.508+30898G>A
Search 100 bp 5'
Search 100 bp 3'