Canonical Allele Identifier: CA1119097434
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816087022

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529806C>A , CM000670.2:g.128529806C>A GRCh38
NC_000008.10:g.129542052C>A , CM000670.1:g.129542052C>A GRCh37
NC_000008.9:g.129611234C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+31264G>T