Canonical Allele Identifier: CA1119102017
Gene: LINC00824 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128555832C>G , CM000670.2:g.128555832C>G GRCh38
NC_000008.10:g.129568078C>G , CM000670.1:g.129568078C>G GRCh37
NC_000008.9:g.129637260C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+5238G>C
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