Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57764147C= , CM000674.2:g.57764147C= | GRCh38 |
| NC_000012.11:g.58157930C= , CM000674.1:g.58157930C= | GRCh37 |
| NC_000012.10:g.56444197C= | NCBI36 |
| NG_007076.1:g.8047G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000785.4:c.1166G= MANE Select | NP_000776.1:p.Arg389= |
| ENST00000228606.9:c.1166G= MANE Select | ENSP00000228606.4:p.Arg389= |
| NM_000785.3:c.1166G= | NP_000776.1:p.Arg389= |
| ENST00000228606.8:c.1166G= | ENSP00000228606.4:p.Arg389= |
| ENST00000546567.5:c.461G= | ENSP00000449472.1:p.Arg154= |
| ENST00000547344.5:n.1305G= | |
| ENST00000713544.1:c.1247G= | ENSP00000518840.1:p.Arg416= |
| ENST00000713545.1:c.*171G= | ENSP00000518841.1:n.*171G= |