Canonical Allele Identifier: CA1119100815
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816372307

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128546870A>T , CM000670.2:g.128546870A>T GRCh38
NC_000008.10:g.129559116A>T , CM000670.1:g.129559116A>T GRCh37
NC_000008.9:g.129628298A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+14200T>A