Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.104034051T= , CM000672.2:g.104034051T= | GRCh38 |
| NC_000010.10:g.105793809T= , CM000672.1:g.105793809T= | GRCh37 |
| NC_000010.9:g.105783799T= | NCBI36 |
| NG_007069.1:g.56830A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000494.4:c.4050A= MANE Select | NP_000485.3:p.Ala1350= |
| ENST00000648076.2:c.4050A= MANE Select | ENSP00000497653.1:p.Ala1350= |
| NM_000494.3:c.4050A= | NP_000485.3:p.Ala1350= |
| ENST00000353479.9:c.4050A= | ENSP00000340937.5:p.Ala1350= |
| ENST00000369733.7:c.3804A= | ENSP00000358748.3:p.Ala1268= |
| ENST00000369733.8:c.3804A= | ENSP00000358748.3:p.Ala1268= |
| ENST00000647647.1:c.80A= |