Canonical Allele Identifier: CA1119097557
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816091644

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128530092C>T , CM000670.2:g.128530092C>T GRCh38
NC_000008.10:g.129542338C>T , CM000670.1:g.129542338C>T GRCh37
NC_000008.9:g.129611520C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+30978G>A