Canonical Allele Identifier: CA1314982479
Gene: LINC01090 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.188083157G= , CM000664.2:g.188083157G= GRCh38
NC_000002.11:g.188947884G= , CM000664.1:g.188947884G= GRCh37
NC_000002.10:g.188656129G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126396.1:n.381-47446C=