Canonical Allele Identifier: CA100366654
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs974630053
MyVariant Identifiers: chr4:g.79589114T>C (hg19) chr4:g.78667960T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667960T>C , CM000666.2:g.78667960T>C GRCh38
NC_000004.11:g.79589114T>C , CM000666.1:g.79589114T>C GRCh37
NC_000004.10:g.79808138T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+4949T>C
NR_038304.1:n.473+4949T>C
NR_038305.1:n.380-5383T>C
NR_038306.1:n.380-12801T>C
NR_038307.1:n.364+4949T>C
NR_038308.1:n.325+4988T>C
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