Canonical Allele Identifier: CA1314982418
Gene: LINC01090 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.188083028A= , CM000664.2:g.188083028A= GRCh38
NC_000002.11:g.188947755A= , CM000664.1:g.188947755A= GRCh37
NC_000002.10:g.188656000A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_126396.1:n.381-47317T=