Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1201699T= , CM000667.2:g.1201699T= | GRCh38 |
| NC_000005.9:g.1201814T= , CM000667.1:g.1201814T= | GRCh37 |
| NC_000005.8:g.1254814T= | NCBI36 |
| NG_008282.1:g.5105T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001003841.3:c.49T= MANE Select | NP_001003841.1:p.Ser17= |
| ENST00000304460.11:c.49T= MANE Select | ENSP00000305302.10:p.Ser17= |
| NM_001003841.2:c.49T= | NP_001003841.1:p.Ser17= |
| ENST00000304460.10:c.49T= | ENSP00000305302.10:p.Ser17= |
| ENST00000515652.5:c.49T= | ENSP00000425701.1:p.Ser17= |