ClinGen Allele Registry
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Canonical Allele Identifier:
CA1119100821
Gene: LINC00824
HGNC
NCBI
Linked Data
dbSNP Id:
rs1816372888
gnomAD v3:
8-128546927-GT-G
gnomAD v4:
8-128546927-GT-G
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.128546929del , CM000670.2:g.128546929del
GRCh38
NC_000008.10:g.129559175del , CM000670.1:g.129559175del
GRCh37
NC_000008.9:g.129628357del
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_121672.1:n.508+14142del
Search 100 bp 5'
Search 100 bp 3'