Canonical Allele Identifier: CA16348818
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs10098821
gnomAD v2: 8-129559228-C-T
gnomAD v3: 8-128546982-C-T
gnomAD v4: 8-128546982-C-T
MyVariant Identifiers: chr8:g.129559228C>T (hg19) chr8:g.128546982C>T (hg38)
Allelic Epigenome: Alellic Epigenome (raw data)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128546982C>T , CM000670.2:g.128546982C>T GRCh38
NC_000008.10:g.129559228C>T , CM000670.1:g.129559228C>T GRCh37
NC_000008.9:g.129628410C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+14088G>A
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