Canonical Allele Identifier: CA1797599583
Gene: LINC02235 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81859804G= , CM000670.2:g.81859804G= GRCh38
NC_000008.10:g.82772039G= , CM000670.1:g.82772039G= GRCh37
NC_000008.9:g.82934594G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170313.1:n.54-13598G=
NR_170314.1:n.223+10697G=
NR_170315.1:n.273-13598G=
NR_170316.1:n.360+5968G=
NR_170317.1:n.481+5968G=
NR_170318.1:n.755+5968G=
NR_170319.1:n.54-3605G=
NR_170320.1:n.616-3605G=