Canonical Allele Identifier: CA214889933

Gene: LINC01153

Linked Data

• dbSNP Id: rs937328189
• MyVariant Identifiers: chr10:g.122939368C>T (hg19) ; chr10:g.121179854C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121179854C>T , CM000672.2:g.121179854C>T	GRCh38
NC_000010.10:g.122939368C>T , CM000672.1:g.122939368C>T	GRCh37
NC_000010.9:g.122929358C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_246197.2:n.684+882C>T