Canonical Allele Identifier: CA1470627175
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs1724949908

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667998T>C , CM000666.2:g.78667998T>C GRCh38
NC_000004.11:g.79589152T>C , CM000666.1:g.79589152T>C GRCh37
NC_000004.10:g.79808176T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+4987T>C
NR_038304.1:n.473+4987T>C
NR_038305.1:n.380-5345T>C
NR_038306.1:n.380-12763T>C
NR_038307.1:n.364+4987T>C
NR_038308.1:n.325+5026T>C