Canonical Allele Identifier: CA552690271
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs1280277945
gnomAD v2: 4-79588866-G-A
gnomAD v3: 4-78667712-G-A
gnomAD v4: 4-78667712-G-A
MyVariant Identifiers: chr4:g.79588866G>A (hg19) chr4:g.78667712G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667712G>A , CM000666.2:g.78667712G>A GRCh38
NC_000004.11:g.79588866G>A , CM000666.1:g.79588866G>A GRCh37
NC_000004.10:g.79807890G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+4701G>A
NR_038304.1:n.473+4701G>A
NR_038305.1:n.380-5631G>A
NR_038306.1:n.380-13049G>A
NR_038307.1:n.364+4701G>A
NR_038308.1:n.325+4740G>A
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