Canonical Allele Identifier: CA2101852555
Gene: LINC00393 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.73492824C= , CM000675.2:g.73492824C= GRCh38
NC_000013.10:g.74066961C= , CM000675.1:g.74066961C= GRCh37
NC_000013.9:g.72964962C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_942061.1:n.379-35862G=