Canonical Allele Identifier: CA100366665
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs79917564
gnomAD v2: 4-79589215-C-G
gnomAD v3: 4-78668061-C-G
gnomAD v4: 4-78668061-C-G
MyVariant Identifiers: chr4:g.79589215C>G (hg19) chr4:g.78668061C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78668061C>G , CM000666.2:g.78668061C>G GRCh38
NC_000004.11:g.79589215C>G , CM000666.1:g.79589215C>G GRCh37
NC_000004.10:g.79808239C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+5050C>G
NR_038304.1:n.473+5050C>G
NR_038305.1:n.380-5282C>G
NR_038306.1:n.380-12700C>G
NR_038307.1:n.364+5050C>G
NR_038308.1:n.325+5089C>G
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