Canonical Allele Identifier: CA847304042

Gene: LINC00824

Linked Data

• dbSNP Id: rs1208732846
• MyVariant Identifiers: chr8:g.129559334T>C (hg19) ; chr8:g.128547088T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128547088T>C , CM000670.2:g.128547088T>C	GRCh38
NC_000008.10:g.129559334T>C , CM000670.1:g.129559334T>C	GRCh37
NC_000008.9:g.129628516T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121672.1:n.508+13982A>G