Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31269165T= , CM000668.2:g.31269165T= | GRCh38 |
| NC_000006.11:g.31236942T= , CM000668.1:g.31236942T= | GRCh37 |
| NC_000006.10:g.31344921T= | NCBI36 |
| NG_029422.2:g.7967A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.*4A= MANE Select | ENSP00000365402.5:n.*4A= | |
| ENST00000376228.9:c.*4A= | ENSP00000365402.5:n.*4A= | |
| ENST00000376237.8:c.*692A= | ENSP00000365412.4:n.*692A= | |
| ENST00000383329.7:c.*4A= | ENSP00000372819.3:n.*4A= | |
| ENST00000466892.5:n.338A= | ||
| ENST00000470363.5:n.863A= | ||
| ENST00000487245.5:n.1464A= | ||
| NM_002117.5:c.*4A= | NP_002108.4:n.*4A= | |
| NM_002117.6:c.*4A= MANE Select | NP_002108.4:n.*4A= |