Canonical Allele Identifier: CA1797599586
Gene: LINC02235 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81859811A= , CM000670.2:g.81859811A= GRCh38
NC_000008.10:g.82772046A= , CM000670.1:g.82772046A= GRCh37
NC_000008.9:g.82934601A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170313.1:n.54-13591A=
NR_170314.1:n.223+10704A=
NR_170315.1:n.273-13591A=
NR_170316.1:n.360+5975A=
NR_170317.1:n.481+5975A=
NR_170318.1:n.755+5975A=
NR_170319.1:n.54-3598A=
NR_170320.1:n.616-3598A=