Canonical Allele Identifier: CA185874161

Gene: LINC00824

Linked Data

• dbSNP Id: rs754948899
• MyVariant Identifiers: chr8:g.129542067T>C (hg19) ; chr8:g.128529821T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128529821T>C , CM000670.2:g.128529821T>C	GRCh38
NC_000008.10:g.129542067T>C , CM000670.1:g.129542067T>C	GRCh37
NC_000008.9:g.129611249T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121672.1:n.508+31249A>G