Canonical Allele Identifier: CA847293982
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs947341696
MyVariant Identifiers: chr8:g.129542107G>T (hg19) chr8:g.128529861G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529861G>T , CM000670.2:g.128529861G>T GRCh38
NC_000008.10:g.129542107G>T , CM000670.1:g.129542107G>T GRCh37
NC_000008.9:g.129611289G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+31209C>A
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