Canonical Allele Identifier: CA1470627192
Gene: LINC01094 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78668059T= , CM000666.2:g.78668059T= GRCh38
NC_000004.11:g.79589213T= , CM000666.1:g.79589213T= GRCh37
NC_000004.10:g.79808237T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+5048T=
NR_038304.1:n.473+5048T=
NR_038305.1:n.380-5284T=
NR_038306.1:n.380-12702T=
NR_038307.1:n.364+5048T=
NR_038308.1:n.325+5087T=