Canonical Allele Identifier: CA585119926
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1324731346
gnomAD v2: 8-129542366-G-C
MyVariant Identifiers: chr8:g.129542366G>C (hg19) chr8:g.128530120G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128530120G>C , CM000670.2:g.128530120G>C GRCh38
NC_000008.10:g.129542366G>C , CM000670.1:g.129542366G>C GRCh37
NC_000008.9:g.129611548G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+30950C>G
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