Canonical Allele Identifier: CA1119097566
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs986482252

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128530125C>T , CM000670.2:g.128530125C>T GRCh38
NC_000008.10:g.129542371C>T , CM000670.1:g.129542371C>T GRCh37
NC_000008.9:g.129611553C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+30945G>A