Canonical Allele Identifier: CA185874177

Gene: LINC00824

Linked Data

• dbSNP Id: rs903323744
• gnomAD v3: 8-128529935-C-T
• gnomAD v4: 8-128529935-C-T
• MyVariant Identifiers: chr8:g.129542181C>T (hg19) ; chr8:g.128529935C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128529935C>T , CM000670.2:g.128529935C>T	GRCh38
NC_000008.10:g.129542181C>T , CM000670.1:g.129542181C>T	GRCh37
NC_000008.9:g.129611363C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121672.1:n.508+31135G>A