Canonical Allele Identifier: CA798766721
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs1266147786
MyVariant Identifiers: chr4:g.79588876G>T (hg19) chr4:g.78667722G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667722G>T , CM000666.2:g.78667722G>T GRCh38
NC_000004.11:g.79588876G>T , CM000666.1:g.79588876G>T GRCh37
NC_000004.10:g.79807900G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038303.1:n.473+4711G>T
NR_038304.1:n.473+4711G>T
NR_038305.1:n.380-5621G>T
NR_038306.1:n.380-13039G>T
NR_038307.1:n.364+4711G>T
NR_038308.1:n.325+4750G>T
Search 100 bp 5'
Search 100 bp 3'