Canonical Allele Identifier: CA1818921162
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816087022

Genomic Alleles

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

Transcript Alleles

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