Canonical Allele Identifier: CA1470627116

Gene: LINC01094

Linked Data

• dbSNP Id: rs1159188252

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78667883T>C , CM000666.2:g.78667883T>C	GRCh38
NC_000004.11:g.79589037T>C , CM000666.1:g.79589037T>C	GRCh37
NC_000004.10:g.79808061T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_038303.1:n.473+4872T>C
NR_038304.1:n.473+4872T>C
NR_038305.1:n.380-5460T>C
NR_038306.1:n.380-12878T>C
NR_038307.1:n.364+4872T>C
NR_038308.1:n.325+4911T>C