Canonical Allele Identifier: CA1818921213
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816088049

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529890G>T , CM000670.2:g.128529890G>T GRCh38
NC_000008.10:g.129542136G>T , CM000670.1:g.129542136G>T GRCh37
NC_000008.9:g.129611318G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+31180C>A