Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.21845237G= , CM000685.2:g.21845237G= | GRCh38 |
| NC_000023.10:g.21863355G= , CM000685.1:g.21863355G= | GRCh37 |
| NC_000023.9:g.21773276G= | NCBI36 |
| NG_012797.1:g.10700G= | |
| NG_012797.2:g.10700G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379484.10:c.291G= MANE Select | ENSP00000368798.5:p.Thr97= | |
| ENST00000365779.2:c.291G= | ENSP00000368796.1:p.Thr97= | |
| ENST00000379484.9:c.291G= | ENSP00000368798.5:p.Thr97= | |
| ENST00000465888.1:n.390G= | ||
| NM_015884.3:c.291G= | NP_056968.1:p.Thr97= | |
| NM_015884.4:c.291G= MANE Select | NP_056968.1:p.Thr97= |