Canonical Allele Identifier: CA100366656
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs770359448
MyVariant Identifiers: chr4:g.79589117G>C (hg19) chr4:g.78667963G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667963G>C , CM000666.2:g.78667963G>C GRCh38
NC_000004.11:g.79589117G>C , CM000666.1:g.79589117G>C GRCh37
NC_000004.10:g.79808141G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+4952G>C
NR_038304.1:n.473+4952G>C
NR_038305.1:n.380-5380G>C
NR_038306.1:n.380-12798G>C
NR_038307.1:n.364+4952G>C
NR_038308.1:n.325+4991G>C
Search 100 bp 5'
Search 100 bp 3'