Canonical Allele Identifier: CA847303952
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1413663593
MyVariant Identifiers: chr8:g.129559213T>C (hg19) chr8:g.128546967T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128546967T>C , CM000670.2:g.128546967T>C GRCh38
NC_000008.10:g.129559213T>C , CM000670.1:g.129559213T>C GRCh37
NC_000008.9:g.129628395T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+14103A>G
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