Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.78123356C>A , CM000685.2:g.78123356C>A | GRCh38 |
| NC_000023.10:g.77378853C>A , CM000685.1:g.77378853C>A | GRCh37 |
| NC_000023.9:g.77265509C>A | NCBI36 |
| NG_008862.1:g.24188C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373316.5:c.918C>A MANE Select | ENSP00000362413.4:p.Gly306= | |
| ENST00000644362.1:c.834C>A | ENSP00000496140.1:p.Gly278= | |
| ENST00000373316.4:c.918C>A | ENSP00000362413.4:p.Gly306= | |
| NM_000291.3:c.918C>A | NP_000282.1:p.Gly306= | |
| NM_000291.4:c.918C>A MANE Select | NP_000282.1:p.Gly306= |