Canonical Allele Identifier: CA1119101200
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816380524

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547229A>G , CM000670.2:g.128547229A>G GRCh38
NC_000008.10:g.129559475A>G , CM000670.1:g.129559475A>G GRCh37
NC_000008.9:g.129628657A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13841T>C