Canonical Allele Identifier: CA185876341
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1055035956
gnomAD v2: 8-129559112-A-T
gnomAD v3: 8-128546866-A-T
gnomAD v4: 8-128546866-A-T
MyVariant Identifiers: chr8:g.129559112A>T (hg19) chr8:g.128546866A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128546866A>T , CM000670.2:g.128546866A>T GRCh38
NC_000008.10:g.129559112A>T , CM000670.1:g.129559112A>T GRCh37
NC_000008.9:g.129628294A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+14204T>A
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