Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.181509807A= , CM000664.2:g.181509807A= | GRCh38 |
| NC_000002.11:g.182374534A= , CM000664.1:g.182374534A= | GRCh37 |
| NC_000002.10:g.182082779A= | NCBI36 |
| NG_050623.1:g.57916A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000885.6:c.1845A= MANE Select | NP_000876.3:p.Thr615= |
| ENST00000397033.7:c.1845A= MANE Select | ENSP00000380227.2:p.Thr615= |
| NM_000885.4:c.1845A= | NP_000876.3:p.Thr615= |
| NM_000885.5:c.1845A= | NP_000876.3:p.Thr615= |
| ENST00000397033.6:c.1845A= | ENSP00000380227.2:p.Thr615= |
| ENST00000476824.1:n.356A= | |
| ENST00000490435.5:n.647A= |