Canonical Allele Identifier: CA2762309517
Gene: LINC01094 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667997T>C , CM000666.2:g.78667997T>C GRCh38
NC_000004.11:g.79589151T>C , CM000666.1:g.79589151T>C GRCh37
NC_000004.10:g.79808175T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+4986T>C
NR_038304.1:n.473+4986T>C
NR_038305.1:n.380-5346T>C
NR_038306.1:n.380-12764T>C
NR_038307.1:n.364+4986T>C
NR_038308.1:n.325+5025T>C