Canonical Allele Identifier: CA1470627055
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs1724943581

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667717T>C , CM000666.2:g.78667717T>C GRCh38
NC_000004.11:g.79588871T>C , CM000666.1:g.79588871T>C GRCh37
NC_000004.10:g.79807895T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+4706T>C
NR_038304.1:n.473+4706T>C
NR_038305.1:n.380-5626T>C
NR_038306.1:n.380-13044T>C
NR_038307.1:n.364+4706T>C
NR_038308.1:n.325+4745T>C