Canonical Allele Identifier: CA1470627058
Gene: LINC01094 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667722G= , CM000666.2:g.78667722G= GRCh38
NC_000004.11:g.79588876G= , CM000666.1:g.79588876G= GRCh37
NC_000004.10:g.79807900G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+4711G=
NR_038304.1:n.473+4711G=
NR_038305.1:n.380-5621G=
NR_038306.1:n.380-13039G=
NR_038307.1:n.364+4711G=
NR_038308.1:n.325+4750G=