| NCBI GeneID : 170062 | NCBI : NM_152631.3 | NCBI : NP_689844.2 |
|---|---|---|
| Chromosome : X | Strand : + | |
| MANE Select : ENST00000329357 | MANE Plus Clinical : |
| Gene Symbol | Ensembl Gene ID | Start | End | |
| MANE | FAM47B | ENSG00000189132 | 34942796 | 34944915 |
|---|---|---|---|---|
| GTEx V8 | FAM47B | ENSG00000189132 | 34942795 | 34944915 |
| Gencode v40 | FAM47B | ENSG00000189132 | 34942795 | 34944915 |
| Gencode v26 (GTEx V8) | Gencode v40 | |||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| V8 |
Transcript ID | Exon Count |
Transcript Length |
Tx Length Rank |
CDS Length |
CDS Rank |
Exp Tx% |
Exp Rank |
MANE Match |
APPRIS | Transcript ID | Exon Count |
Transcript Length |
Tx Length Rank |
CDS Length |
CDS Rank |
MANE Match |
APPRIS |
| ☉ | ENST00000329357 | 1 | 2120 | 1 | 1938 | 1 | 100.00 | 1 | ☀ | P:1 | ENST00000329357 | 1 | 2120 | 1 | 1938 | 1 | ☀ | P:1 |