Canonical Allele Identifier: CA700785426

Gene: LINC00393

Linked Data

• dbSNP Id: rs1463511507
• MyVariant Identifiers: chr13:g.74066950A>G (hg19) ; chr13:g.73492813A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.73492813A>G , CM000675.2:g.73492813A>G	GRCh38
NC_000013.10:g.74066950A>G , CM000675.1:g.74066950A>G	GRCh37
NC_000013.9:g.72964951A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_942061.1:n.379-35851T>C