Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.44506715G>A , CM000676.2:g.44506715G>A | GRCh38 |
| NC_000014.8:g.44975918G>A , CM000676.1:g.44975918G>A | GRCh37 |
| NC_000014.7:g.44045668G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_032135.4:c.273C>T (FSCB) MANE Select | NP_115511.3:p.Thr91= |
| ENST00000340446.5:c.273C>T (FSCB) MANE Select | ENSP00000344579.4:p.Thr91= |
| NM_032135.3:c.273C>T (FSCB) | NP_115511.3:p.Thr91= |
| ENST00000340446.4:c.273C>T (FSCB) | ENSP00000344579.4:p.Thr91= |
| XR_943800.1:n.331-61893C>T (LINC02302) | |
| XR_943801.1:n.330+90194C>T (LINC02302) | |
| XR_943806.1:n.331-61893C>T (LINC02302) | |
| XR_943808.1:n.127-112977C>T (LINC02302) |