Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186672550T= , CM000663.2:g.186672550T= | GRCh38 |
| NC_000001.10:g.186641682T= , CM000663.1:g.186641682T= | GRCh37 |
| NC_000001.9:g.184908305T= | NCBI36 |
| NG_028206.2:g.12878A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000963.4:c.*1803A= MANE Select | NP_000954.1:n.*1803A= |
| ENST00000367468.10:c.*1803A= MANE Select | ENSP00000356438.5:n.*1803A= |
| NM_000963.3:c.*1803A= | NP_000954.1:n.*1803A= |
| ENST00000367468.9:c.*1803A= | ENSP00000356438.5:n.*1803A= |
| ENST00000680451.1:c.*1803A= | ENSP00000506242.1:n.*1803A= |
| ENST00000681605.1:c.*3290A= | ENSP00000504900.1:n.*3290A= |