Canonical Allele Identifier: CA1119097598

Gene: LINC00824

Linked Data

• dbSNP Id: rs1816093129
• gnomAD v3: 8-128530177-C-T
• gnomAD v4: 8-128530177-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128530177C>T , CM000670.2:g.128530177C>T	GRCh38
NC_000008.10:g.129542423C>T , CM000670.1:g.129542423C>T	GRCh37
NC_000008.9:g.129611605C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121672.1:n.508+30893G>A