Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87743589C= , CM000672.2:g.87743589C= | GRCh38 |
| NC_000010.10:g.89503346C= , CM000672.1:g.89503346C= | GRCh37 |
| NC_000010.9:g.89493326C= | NCBI36 |
| NG_012150.1:g.88871C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001015880.2:c.1439C= MANE Select | NP_001015880.1:p.Ser480= |
| ENST00000456849.2:c.1439C= MANE Select | ENSP00000406157.1:p.Ser480= |
| NM_001015880.1:c.1439C= | NP_001015880.1:p.Ser480= |
| NM_004670.3:c.1424C= | NP_004661.2:p.Ser475= |
| NM_004670.4:c.1424C= | NP_004661.2:p.Ser475= |
| ENST00000361175.8:c.1424C= | ENSP00000354436.4:p.Ser475= |
| ENST00000456849.1:c.1439C= | ENSP00000406157.1:p.Ser480= |