Canonical Allele Identifier: CA1818921216
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816088107

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529892T>C , CM000670.2:g.128529892T>C GRCh38
NC_000008.10:g.129542138T>C , CM000670.1:g.129542138T>C GRCh37
NC_000008.9:g.129611320T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+31178A>G