ClinGen Allele Registry
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Canonical Allele Identifier:
CA185874202
Gene: LINC00824
HGNC
NCBI
Linked Data
dbSNP Id:
rs867824532
gnomAD v2:
8-129542281-T-A
gnomAD v3:
8-128530035-T-A
gnomAD v4:
8-128530035-T-A
MyVariant Identifiers:
chr8:g.129542281T>A (hg19)
chr8:g.128530035T>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.128530035T>A , CM000670.2:g.128530035T>A
GRCh38
NC_000008.10:g.129542281T>A , CM000670.1:g.129542281T>A
GRCh37
NC_000008.9:g.129611463T>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_121672.1:n.508+31035A>T
Search 100 bp 5'
Search 100 bp 3'