Canonical Allele Identifier: CA1818921237
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816088511
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529920A>G , CM000670.2:g.128529920A>G GRCh38
NC_000008.10:g.129542166A>G , CM000670.1:g.129542166A>G GRCh37
NC_000008.9:g.129611348A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+31150T>C
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