Canonical Allele Identifier: CA1064495919
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs1724943191
gnomAD v3: 4-78667704-C-G
gnomAD v4: 4-78667704-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667704C>G , CM000666.2:g.78667704C>G GRCh38
NC_000004.11:g.79588858C>G , CM000666.1:g.79588858C>G GRCh37
NC_000004.10:g.79807882C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+4693C>G
NR_038304.1:n.473+4693C>G
NR_038305.1:n.380-5639C>G
NR_038306.1:n.380-13057C>G
NR_038307.1:n.364+4693C>G
NR_038308.1:n.325+4732C>G