Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7934040T= , CM000681.2:g.7934040T= | GRCh38 |
| NC_000019.9:g.7998925T= , CM000681.1:g.7998925T= | GRCh37 |
| NC_000019.8:g.7904925T= | NCBI36 |
| NG_051180.1:g.14784A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270538.8:c.544-37A= MANE Select | ENSP00000270538.2:n.544-37A= | |
| ENST00000270538.7:c.544-37A= | ENSP00000270538.2:n.544-37A= | |
| ENST00000595831.5:c.531-37A= | ||
| ENST00000595876.5:c.*232-37A= | ENSP00000471596.1:n.*232-37A= | |
| ENST00000597926.1:c.448-37A= | ENSP00000469389.1:n.448-37A= | |
| ENST00000600748.5:n.529-37A= | ||
| NM_006351.3:c.544-37A= | NP_006342.2:n.544-37A= | |
| NM_006351.4:c.544-37A= MANE Select | NP_006342.2:n.544-37A= |