Canonical Allele Identifier: CA1119097429
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816086684

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529790C>T , CM000670.2:g.128529790C>T GRCh38
NC_000008.10:g.129542036C>T , CM000670.1:g.129542036C>T GRCh37
NC_000008.9:g.129611218C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+31280G>A