Canonical Allele Identifier: CA1064496006
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs1724950434
gnomAD v3: 4-78668028-G-C
gnomAD v4: 4-78668028-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78668028G>C , CM000666.2:g.78668028G>C GRCh38
NC_000004.11:g.79589182G>C , CM000666.1:g.79589182G>C GRCh37
NC_000004.10:g.79808206G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+5017G>C
NR_038304.1:n.473+5017G>C
NR_038305.1:n.380-5315G>C
NR_038306.1:n.380-12733G>C
NR_038307.1:n.364+5017G>C
NR_038308.1:n.325+5056G>C
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