Canonical Allele Identifier: CA185874175

Gene: LINC00824

Linked Data

• dbSNP Id: rs1057211836
• MyVariant Identifiers: chr8:g.129542173A>G (hg19) ; chr8:g.128529927A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128529927A>G , CM000670.2:g.128529927A>G	GRCh38
NC_000008.10:g.129542173A>G , CM000670.1:g.129542173A>G	GRCh37
NC_000008.9:g.129611355A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121672.1:n.508+31143T>C