Canonical Allele Identifier: CA1470627150
Gene: LINC01094 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667948T= , CM000666.2:g.78667948T= GRCh38
NC_000004.11:g.79589102T= , CM000666.1:g.79589102T= GRCh37
NC_000004.10:g.79808126T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+4937T=
NR_038304.1:n.473+4937T=
NR_038305.1:n.380-5395T=
NR_038306.1:n.380-12813T=
NR_038307.1:n.364+4937T=
NR_038308.1:n.325+4976T=