Canonical Allele Identifier: CA1818922565
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128531621G= , CM000670.2:g.128531621G= GRCh38
NC_000008.10:g.129543867G= , CM000670.1:g.129543867G= GRCh37
NC_000008.9:g.129613049G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+29449C=