Canonical Allele Identifier: CA185874451

Gene: LINC00824

Linked Data

• dbSNP Id: rs899301126
• COSMIC: COSN19517961
• MyVariant Identifiers: chr8:g.129544016C>T (hg19) ; chr8:g.128531770C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128531770C>T , CM000670.2:g.128531770C>T	GRCh38
NC_000008.10:g.129544016C>T , CM000670.1:g.129544016C>T	GRCh37
NC_000008.9:g.129613198C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121672.1:n.508+29300G>A