Canonical Allele Identifier: CA185874158

Gene: LINC00824

Linked Data

• dbSNP Id: rs971859450
• MyVariant Identifiers: chr8:g.129542041A>C (hg19) ; chr8:g.128529795A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128529795A>C , CM000670.2:g.128529795A>C	GRCh38
NC_000008.10:g.129542041A>C , CM000670.1:g.129542041A>C	GRCh37
NC_000008.9:g.129611223A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_121672.1:n.508+31275T>G