Canonical Allele Identifier: CA1470627163
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs1724949325

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667967T>C , CM000666.2:g.78667967T>C GRCh38
NC_000004.11:g.79589121T>C , CM000666.1:g.79589121T>C GRCh37
NC_000004.10:g.79808145T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+4956T>C
NR_038304.1:n.473+4956T>C
NR_038305.1:n.380-5376T>C
NR_038306.1:n.380-12794T>C
NR_038307.1:n.364+4956T>C
NR_038308.1:n.325+4995T>C