Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.6778379T= , CM000682.2:g.6778379T= | GRCh38 |
| NC_000020.10:g.6759026T= , CM000682.1:g.6759026T= | GRCh37 |
| NC_000020.9:g.6707026T= | NCBI36 |
| NG_023233.1:g.15282T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000378827.5:c.481T= MANE Select | ENSP00000368104.3:p.Leu161= | |
| ENST00000378827.4:c.481T= | ENSP00000368104.3:p.Leu161= | |
| NM_001200.2:c.481T= | NP_001191.1:p.Leu161= | |
| XM_011529323.1:c.13T= | XP_011527625.1:p.Leu5= | |
| NM_001200.3:c.481T= | NP_001191.1:p.Leu161= | |
| NM_001200.4:c.481T= MANE Select | NP_001191.1:p.Leu161= |