Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.161219139T= , CM000663.2:g.161219139T= | GRCh38 |
| NC_000001.10:g.161188929T= , CM000663.1:g.161188929T= | GRCh37 |
| NC_000001.9:g.159455553T= | NCBI36 |
| NG_029043.1:g.8843T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000289902.2:c.*196T= MANE Select | ENSP00000289902.1:n.*196T= | |
| ENST00000289902.1:c.*196T= | ENSP00000289902.1:n.*196T= | |
| ENST00000367992.7:c.198+416T= | ENSP00000356971.3:n.198+416T= | |
| ENST00000490414.1:n.453T= | ||
| NM_004106.1:c.*196T= | NP_004097.1:n.*196T= | |
| NM_004106.2:c.*196T= MANE Select | NP_004097.1:n.*196T= |