Canonical Allele Identifier: CA847303937

Gene: LINC00824

Linked Data

• dbSNP Id: rs1276789183
• MyVariant Identifiers: chr8:g.129559181T>C (hg19) ; chr8:g.128546935T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128546935T>C , CM000670.2:g.128546935T>C	GRCh38
NC_000008.10:g.129559181T>C , CM000670.1:g.129559181T>C	GRCh37
NC_000008.9:g.129628363T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_121672.1:n.508+14135A>G