Canonical Allele Identifier: CA1470627082
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs1044074040

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667785A>T , CM000666.2:g.78667785A>T GRCh38
NC_000004.11:g.79588939A>T , CM000666.1:g.79588939A>T GRCh37
NC_000004.10:g.79807963A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+4774A>T
NR_038304.1:n.473+4774A>T
NR_038305.1:n.380-5558A>T
NR_038306.1:n.380-12976A>T
NR_038307.1:n.364+4774A>T
NR_038308.1:n.325+4813A>T