Canonical Allele Identifier: CA100366644
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs965585701
MyVariant Identifiers: chr4:g.79589042C>T (hg19) chr4:g.78667888C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667888C>T , CM000666.2:g.78667888C>T GRCh38
NC_000004.11:g.79589042C>T , CM000666.1:g.79589042C>T GRCh37
NC_000004.10:g.79808066C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038303.1:n.473+4877C>T
NR_038304.1:n.473+4877C>T
NR_038305.1:n.380-5455C>T
NR_038306.1:n.380-12873C>T
NR_038307.1:n.364+4877C>T
NR_038308.1:n.325+4916C>T
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