Canonical Allele Identifier: CA1040357698
Gene: LINC01090 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.188083014A>C , CM000664.2:g.188083014A>C GRCh38
NC_000002.11:g.188947741A>C , CM000664.1:g.188947741A>C GRCh37
NC_000002.10:g.188655986A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126396.1:n.381-47303T>G