Canonical Allele Identifier: CA2782164965
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529850A>T , CM000670.2:g.128529850A>T GRCh38
NC_000008.10:g.129542096A>T , CM000670.1:g.129542096A>T GRCh37
NC_000008.9:g.129611278A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+31220T>A