Canonical Allele Identifier: CA1470627158
Gene: LINC01094 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667960T= , CM000666.2:g.78667960T= GRCh38
NC_000004.11:g.79589114T= , CM000666.1:g.79589114T= GRCh37
NC_000004.10:g.79808138T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+4949T=
NR_038304.1:n.473+4949T=
NR_038305.1:n.380-5383T=
NR_038306.1:n.380-12801T=
NR_038307.1:n.364+4949T=
NR_038308.1:n.325+4988T=