Canonical Allele Identifier: CA1470627178
Gene: LINC01094 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78668006T= , CM000666.2:g.78668006T= GRCh38
NC_000004.11:g.79589160T= , CM000666.1:g.79589160T= GRCh37
NC_000004.10:g.79808184T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+4995T=
NR_038304.1:n.473+4995T=
NR_038305.1:n.380-5337T=
NR_038306.1:n.380-12755T=
NR_038307.1:n.364+4995T=
NR_038308.1:n.325+5034T=