Canonical Allele Identifier: CA847303905

Gene: LINC00824

Linked Data

• dbSNP Id: rs1425414938
• MyVariant Identifiers: chr8:g.129559126G>A (hg19) ; chr8:g.128546880G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128546880G>A , CM000670.2:g.128546880G>A	GRCh38
NC_000008.10:g.129559126G>A , CM000670.1:g.129559126G>A	GRCh37
NC_000008.9:g.129628308G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121672.1:n.508+14190C>T