ClinGen Allele Registry
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Canonical Allele Identifier:
CA185874441
Gene: LINC00824
HGNC
NCBI
Linked Data
dbSNP Id:
rs1054147869
gnomAD v2:
8-129543973-C-A
gnomAD v3:
8-128531727-C-A
gnomAD v4:
8-128531727-C-A
MyVariant Identifiers:
chr8:g.129543973C>A (hg19)
chr8:g.128531727C>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.128531727C>A , CM000670.2:g.128531727C>A
GRCh38
NC_000008.10:g.129543973C>A , CM000670.1:g.129543973C>A
GRCh37
NC_000008.9:g.129613155C>A
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_121672.1:n.508+29343G>T
Search 100 bp 5'
Search 100 bp 3'