Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1415514A= , CM000667.2:g.1415514A= | GRCh38 |
| NC_000005.9:g.1415629A= , CM000667.1:g.1415629A= | GRCh37 |
| NC_000005.8:g.1468629A= | NCBI36 |
| NG_015885.1:g.34915T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001044.5:c.1031+584T= MANE Select | NP_001035.1:n.1031+584T= |
| ENST00000270349.12:c.1031+584T= MANE Select | ENSP00000270349.9:n.1031+584T= |
| NM_001044.4:c.1031+584T= | NP_001035.1:n.1031+584T= |
| ENST00000270349.11:c.1031+584T= | ENSP00000270349.9:n.1031+584T= |
| ENST00000511750.1:n.481+584T= |