Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42909355T= , CM000679.2:g.42909355T= | GRCh38 |
| NC_000017.10:g.41061372T= , CM000679.1:g.41061372T= | GRCh37 |
| NC_000017.9:g.38314898T= | NCBI36 |
| NG_011808.1:g.13558T= , LRG_147:g.13558T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000151.4:c.499T= MANE Select | NP_000142.2:p.Cys167= |
| ENST00000253801.7:c.499T= MANE Select | ENSP00000253801.1:p.Cys167= |
| NM_000151.3:c.499T= | NP_000142.2:p.Cys167= |
| NM_001270397.1:c.422T= | NP_001257326.1:p.Leu141= |
| NM_001270397.2:c.422T= | NP_001257326.1:p.Leu141= |
| ENST00000253801.6:c.499T= | ENSP00000253801.1:p.Cys167= |
| ENST00000585489.1:c.447-1560T= | ENSP00000466202.1:n.447-1560T= |
| ENST00000592383.5:c.422T= | ENSP00000465958.1:p.Leu141= |