Canonical Allele Identifier: CA2101852559
Gene: LINC00393 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.73492841A= , CM000675.2:g.73492841A= GRCh38
NC_000013.10:g.74066978A= , CM000675.1:g.74066978A= GRCh37
NC_000013.9:g.72964979A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_942061.1:n.379-35879T=