Canonical Allele Identifier: CA2718093185
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs138100460

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128554856C>T , CM000670.2:g.128554856C>T GRCh38
NC_000008.10:g.129567102C>T , CM000670.1:g.129567102C>T GRCh37
NC_000008.9:g.129636284C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+6214G>A