Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.78124896G= , CM000685.2:g.78124896G= | GRCh38 |
| NC_000023.10:g.77380393G= , CM000685.1:g.77380393G= | GRCh37 |
| NC_000023.9:g.77267049G= | NCBI36 |
| NG_008862.1:g.25728G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000291.4:c.959G= MANE Select | NP_000282.1:p.Ser320= |
| ENST00000373316.5:c.959G= MANE Select | ENSP00000362413.4:p.Ser320= |
| NM_000291.3:c.959G= | NP_000282.1:p.Ser320= |
| ENST00000373316.4:c.959G= | ENSP00000362413.4:p.Ser320= |
| ENST00000644362.1:c.875G= | ENSP00000496140.1:p.Ser292= |