Canonical Allele Identifier: CA762147089
Gene: LINC01090 HGNC NCBI

Linked Data

dbSNP Id: rs1414045273

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.188083139C>G , CM000664.2:g.188083139C>G GRCh38
NC_000002.11:g.188947866C>G , CM000664.1:g.188947866C>G GRCh37
NC_000002.10:g.188656111C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126396.1:n.381-47428G>C