Canonical Allele Identifier: CA100366658
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs946645092
gnomAD v2: 4-79589128-T-C
gnomAD v3: 4-78667974-T-C
gnomAD v4: 4-78667974-T-C
MyVariant Identifiers: chr4:g.79589128T>C (hg19) chr4:g.78667974T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667974T>C , CM000666.2:g.78667974T>C GRCh38
NC_000004.11:g.79589128T>C , CM000666.1:g.79589128T>C GRCh37
NC_000004.10:g.79808152T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+4963T>C
NR_038304.1:n.473+4963T>C
NR_038305.1:n.380-5369T>C
NR_038306.1:n.380-12787T>C
NR_038307.1:n.364+4963T>C
NR_038308.1:n.325+5002T>C
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