Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.193251846T= , CM000663.2:g.193251846T= | GRCh38 |
| NC_000001.10:g.193220976T= , CM000663.1:g.193220976T= | GRCh37 |
| NC_000001.9:g.191487599T= | NCBI36 |
| NG_012691.1:g.134889T= , LRG_507:g.134889T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367435.5:c.*1134T= MANE Select | ENSP00000356405.4:n.*1134T= | |
| ENST00000635846.1:c.*1134T= | ENSP00000490035.1:n.*1134T= | |
| ENST00000643006.1:c.*1640T= | ENSP00000496633.1:n.*1640T= | |
| ENST00000367435.3:c.*1134T= | ENSP00000356405.3:n.*1134T= | |
| NM_024529.4:c.*1134T= , LRG_507t1:c.*1134T= | NP_078805.3:n.*1134T= | |
| NM_024529.5:c.*1134T= MANE Select | NP_078805.3:n.*1134T= |