Canonical Allele Identifier: CA1470627095
Gene: LINC01094 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667811T= , CM000666.2:g.78667811T= GRCh38
NC_000004.11:g.79588965T= , CM000666.1:g.79588965T= GRCh37
NC_000004.10:g.79807989T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038303.1:n.473+4800T=
NR_038304.1:n.473+4800T=
NR_038305.1:n.380-5532T=
NR_038306.1:n.380-12950T=
NR_038307.1:n.364+4800T=
NR_038308.1:n.325+4839T=