Canonical Allele Identifier: CA2101852549
Gene: LINC00393 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.73492798A= , CM000675.2:g.73492798A= GRCh38
NC_000013.10:g.74066935A= , CM000675.1:g.74066935A= GRCh37
NC_000013.9:g.72964936A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_942061.1:n.379-35836T=