Canonical Allele Identifier: CA1818921106
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529725T= , CM000670.2:g.128529725T= GRCh38
NC_000008.10:g.129541971T= , CM000670.1:g.129541971T= GRCh37
NC_000008.9:g.129611153T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+31345A=