Canonical Allele Identifier: CA185876352
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs570079826
MyVariant Identifiers: chr8:g.129559193C>T (hg19) chr8:g.128546947C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128546947C>T , CM000670.2:g.128546947C>T GRCh38
NC_000008.10:g.129559193C>T , CM000670.1:g.129559193C>T GRCh37
NC_000008.9:g.129628375C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+14123G>A
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