Canonical Allele Identifier: CA1818921479
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128530191T= , CM000670.2:g.128530191T= GRCh38
NC_000008.10:g.129542437T= , CM000670.1:g.129542437T= GRCh37
NC_000008.9:g.129611619T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+30879A=