Canonical Allele Identifier: CA798766846
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs1255610867
MyVariant Identifiers: chr4:g.79589039del (hg19) chr4:g.78667885del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667889del , CM000666.2:g.78667889del GRCh38
NC_000004.11:g.79589043del , CM000666.1:g.79589043del GRCh37
NC_000004.10:g.79808067del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+4878del
NR_038304.1:n.473+4878del
NR_038305.1:n.380-5454del
NR_038306.1:n.380-12872del
NR_038307.1:n.364+4878del
NR_038308.1:n.325+4917del
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