Canonical Allele Identifier: CA100366651
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs548106923
gnomAD v3: 4-78667946-A-G
gnomAD v4: 4-78667946-A-G
MyVariant Identifiers: chr4:g.79589100A>G (hg19) chr4:g.78667946A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667946A>G , CM000666.2:g.78667946A>G GRCh38
NC_000004.11:g.79589100A>G , CM000666.1:g.79589100A>G GRCh37
NC_000004.10:g.79808124A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038303.1:n.473+4935A>G
NR_038304.1:n.473+4935A>G
NR_038305.1:n.380-5397A>G
NR_038306.1:n.380-12815A>G
NR_038307.1:n.364+4935A>G
NR_038308.1:n.325+4974A>G
Search 100 bp 5'
Search 100 bp 3'