Canonical Allele Identifier: CA1119097421
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816086551

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529773G>A , CM000670.2:g.128529773G>A GRCh38
NC_000008.10:g.129542019G>A , CM000670.1:g.129542019G>A GRCh37
NC_000008.9:g.129611201G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+31297C>T