Canonical Allele Identifier: CA2782165621
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547228T>G , CM000670.2:g.128547228T>G GRCh38
NC_000008.10:g.129559474T>G , CM000670.1:g.129559474T>G GRCh37
NC_000008.9:g.129628656T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13842A>C