Canonical Allele Identifier: CA660801786

Gene: LINC01153

Linked Data

• dbSNP Id: rs1180479447
• MyVariant Identifiers: chr10:g.122939379T>A (hg19) ; chr10:g.121179865T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121179865T>A , CM000672.2:g.121179865T>A	GRCh38
NC_000010.10:g.122939379T>A , CM000672.1:g.122939379T>A	GRCh37
NC_000010.9:g.122929369T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_246197.2:n.684+893T>A