Canonical Allele Identifier: CA2753560975
Gene: LINC01090 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.188083130G>T , CM000664.2:g.188083130G>T GRCh38
NC_000002.11:g.188947857G>T , CM000664.1:g.188947857G>T GRCh37
NC_000002.10:g.188656102G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_126396.1:n.381-47419C>A