Canonical Allele Identifier: CA1797599623
Gene: LINC02235 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81859897C= , CM000670.2:g.81859897C= GRCh38
NC_000008.10:g.82772132C= , CM000670.1:g.82772132C= GRCh37
NC_000008.9:g.82934687C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170313.1:n.54-13505C=
NR_170314.1:n.223+10790C=
NR_170315.1:n.273-13505C=
NR_170316.1:n.360+6061C=
NR_170317.1:n.481+6061C=
NR_170318.1:n.755+6061C=
NR_170319.1:n.54-3512C=
NR_170320.1:n.616-3512C=