Canonical Allele Identifier: CA214889942

Gene: LINC01153

Linked Data

• dbSNP Id: rs886861202
• MyVariant Identifiers: chr10:g.122939438C>G (hg19) ; chr10:g.121179924C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121179924C>G , CM000672.2:g.121179924C>G	GRCh38
NC_000010.10:g.122939438C>G , CM000672.1:g.122939438C>G	GRCh37
NC_000010.9:g.122929428C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_246197.2:n.684+952C>G