Canonical Allele Identifier: CA2101852534
Gene: LINC00393 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.73492776G= , CM000675.2:g.73492776G= GRCh38
NC_000013.10:g.74066913G= , CM000675.1:g.74066913G= GRCh37
NC_000013.9:g.72964914G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_942061.1:n.379-35814C=