Canonical Allele Identifier: CA2706318864
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs2109856400

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667935G>A , CM000666.2:g.78667935G>A GRCh38
NC_000004.11:g.79589089G>A , CM000666.1:g.79589089G>A GRCh37
NC_000004.10:g.79808113G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+4924G>A
NR_038304.1:n.473+4924G>A
NR_038305.1:n.380-5408G>A
NR_038306.1:n.380-12826G>A
NR_038307.1:n.364+4924G>A
NR_038308.1:n.325+4963G>A