Canonical Allele Identifier: CA2494526734
Gene: LINC01833 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44927769G>T , CM000664.2:g.44927769G>T GRCh38
NC_000002.11:g.45154908G>T , CM000664.1:g.45154908G>T GRCh37
NC_000002.10:g.45008412G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_147195.1:n.378-4190C>A