Canonical Allele Identifier: CA2101852540
Gene: LINC00393 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.73492782C= , CM000675.2:g.73492782C= GRCh38
NC_000013.10:g.74066919C= , CM000675.1:g.74066919C= GRCh37
NC_000013.9:g.72964920C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_942061.1:n.379-35820G=