Canonical Allele Identifier: CA798766932
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs1219209211
MyVariant Identifiers: chr4:g.79589125A>T (hg19) chr4:g.78667971A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667971A>T , CM000666.2:g.78667971A>T GRCh38
NC_000004.11:g.79589125A>T , CM000666.1:g.79589125A>T GRCh37
NC_000004.10:g.79808149A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+4960A>T
NR_038304.1:n.473+4960A>T
NR_038305.1:n.380-5372A>T
NR_038306.1:n.380-12790A>T
NR_038307.1:n.364+4960A>T
NR_038308.1:n.325+4999A>T
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