Canonical Allele Identifier: CA1818909601
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547227A= , CM000670.2:g.128547227A= GRCh38
NC_000008.10:g.129559473A= , CM000670.1:g.129559473A= GRCh37
NC_000008.9:g.129628655A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13843T=