Canonical Allele Identifier: CA100366628
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs925811355
gnomAD v2: 4-79588881-A-T
gnomAD v3: 4-78667727-A-T
gnomAD v4: 4-78667727-A-T
MyVariant Identifiers: chr4:g.79588881A>T (hg19) chr4:g.78667727A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667727A>T , CM000666.2:g.78667727A>T GRCh38
NC_000004.11:g.79588881A>T , CM000666.1:g.79588881A>T GRCh37
NC_000004.10:g.79807905A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+4716A>T
NR_038304.1:n.473+4716A>T
NR_038305.1:n.380-5616A>T
NR_038306.1:n.380-13034A>T
NR_038307.1:n.364+4716A>T
NR_038308.1:n.325+4755A>T
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