Canonical Allele Identifier: CA798766829
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs1159188252
gnomAD v3: 4-78667883-T-G
gnomAD v4: 4-78667883-T-G
MyVariant Identifiers: chr4:g.79589037T>G (hg19) chr4:g.78667883T>G (hg38)
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Genomic Alleles

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

Transcript Alleles

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