Canonical Allele Identifier: CA1470627069
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs1724944331

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667751C>A , CM000666.2:g.78667751C>A GRCh38
NC_000004.11:g.79588905C>A , CM000666.1:g.79588905C>A GRCh37
NC_000004.10:g.79807929C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+4740C>A
NR_038304.1:n.473+4740C>A
NR_038305.1:n.380-5592C>A
NR_038306.1:n.380-13010C>A
NR_038307.1:n.364+4740C>A
NR_038308.1:n.325+4779C>A