Canonical Allele Identifier: CA1119100827
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816373397

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128546976A>G , CM000670.2:g.128546976A>G GRCh38
NC_000008.10:g.129559222A>G , CM000670.1:g.129559222A>G GRCh37
NC_000008.9:g.129628404A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+14094T>C