Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18386331T= , CM000681.2:g.18386331T= | GRCh38 |
| NC_000019.9:g.18497141T= , CM000681.1:g.18497141T= | GRCh37 |
| NC_000019.8:g.18358141T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004864.4:c.142T= MANE Select | NP_004855.2:p.Ser48= |
| ENST00000252809.3:c.142T= MANE Select | ENSP00000252809.3:p.Ser48= |
| NM_004864.2:c.142T= | NP_004855.2:p.Ser48= |
| NM_004864.3:c.142T= | NP_004855.2:p.Ser48= |
| ENST00000595973.2:c.142T= | ENSP00000470531.2:p.Ser48= |
| ENST00000595973.3:c.142T= | ENSP00000470531.3:p.Ser48= |
| ENST00000597765.2:c.142T= | ENSP00000469819.2:p.Ser48= |
| XM_024451789.1:c.142T= | XP_024307557.1:p.Ser48= |