Canonical Allele Identifier: CA2101852554
Gene: LINC00393 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.73492822T= , CM000675.2:g.73492822T= GRCh38
NC_000013.10:g.74066959T= , CM000675.1:g.74066959T= GRCh37
NC_000013.9:g.72964960T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_942061.1:n.379-35860A=