Canonical Allele Identifier: CA185876368
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs185602792
MyVariant Identifiers: chr8:g.129559293A>C (hg19) chr8:g.128547047A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547047A>C , CM000670.2:g.128547047A>C GRCh38
NC_000008.10:g.129559293A>C , CM000670.1:g.129559293A>C GRCh37
NC_000008.9:g.129628475A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+14023T>G
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