Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186673855C= , CM000663.2:g.186673855C= | GRCh38 |
| NC_000001.10:g.186642987C= , CM000663.1:g.186642987C= | GRCh37 |
| NC_000001.9:g.184909610C= | NCBI36 |
| NG_028206.2:g.11573G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367468.10:c.*498G= MANE Select | ENSP00000356438.5:n.*498G= | |
| ENST00000680451.1:c.*498G= | ENSP00000506242.1:n.*498G= | |
| ENST00000681605.1:c.*1985G= | ENSP00000504900.1:n.*1985G= | |
| ENST00000367468.9:c.*498G= | ENSP00000356438.5:n.*498G= | |
| ENST00000490885.6:n.2728G= | ||
| NM_000963.3:c.*498G= | NP_000954.1:n.*498G= | |
| NM_000963.4:c.*498G= MANE Select | NP_000954.1:n.*498G= |