Canonical Allele Identifier: CA124153840
Gene: LINC00492 HGNC NCBI
LINC00491 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.102611094A>G , CM000667.2:g.102611094A>G GRCh38
NC_000005.9:g.101946798A>G , CM000667.1:g.101946798A>G GRCh37
NC_000005.8:g.101974697A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_047462.1:n.200-6102A>G (LINC00492)
NR_103753.1:n.388-1328T>C (LINC00491)
NR_103754.1:n.372+799T>C (LINC00491)
NR_103755.1:n.310-1328T>C (LINC00491)
NR_103756.1:n.239-1328T>C (LINC00491)