Canonical Allele Identifier: CA2718331658
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs2130614171
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128546931T>C , CM000670.2:g.128546931T>C GRCh38
NC_000008.10:g.129559177T>C , CM000670.1:g.129559177T>C GRCh37
NC_000008.9:g.129628359T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+14139A>G
Search 100 bp 5'
Search 100 bp 3'