Canonical Allele Identifier: CA2706318866
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs2109856500

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78668055C>T , CM000666.2:g.78668055C>T GRCh38
NC_000004.11:g.79589209C>T , CM000666.1:g.79589209C>T GRCh37
NC_000004.10:g.79808233C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+5044C>T
NR_038304.1:n.473+5044C>T
NR_038305.1:n.380-5288C>T
NR_038306.1:n.380-12706C>T
NR_038307.1:n.364+5044C>T
NR_038308.1:n.325+5083C>T