Canonical Allele Identifier: CA100366659
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs570027001
gnomAD v3: 4-78667988-G-A
gnomAD v4: 4-78667988-G-A
MyVariant Identifiers: chr4:g.79589142G>A (hg19) chr4:g.78667988G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667988G>A , CM000666.2:g.78667988G>A GRCh38
NC_000004.11:g.79589142G>A , CM000666.1:g.79589142G>A GRCh37
NC_000004.10:g.79808166G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+4977G>A
NR_038304.1:n.473+4977G>A
NR_038305.1:n.380-5355G>A
NR_038306.1:n.380-12773G>A
NR_038307.1:n.364+4977G>A
NR_038308.1:n.325+5016G>A
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