Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.193251595T= , CM000663.2:g.193251595T= | GRCh38 |
| NC_000001.10:g.193220725T= , CM000663.1:g.193220725T= | GRCh37 |
| NC_000001.9:g.191487348T= | NCBI36 |
| NG_012691.1:g.134638T= , LRG_507:g.134638T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367435.5:c.*883T= MANE Select | ENSP00000356405.4:n.*883T= | |
| ENST00000635846.1:c.*883T= | ENSP00000490035.1:n.*883T= | |
| ENST00000643006.1:c.*1389T= | ENSP00000496633.1:n.*1389T= | |
| ENST00000367435.3:c.*883T= | ENSP00000356405.3:n.*883T= | |
| NM_024529.4:c.*883T= , LRG_507t1:c.*883T= | NP_078805.3:n.*883T= | |
| NM_024529.5:c.*883T= MANE Select | NP_078805.3:n.*883T= |