Canonical Allele Identifier: CA585113117
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1201272080

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128554845C>T , CM000670.2:g.128554845C>T GRCh38
NC_000008.10:g.129567091C>T , CM000670.1:g.129567091C>T GRCh37
NC_000008.9:g.129636273C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+6225G>A