Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154969518C= , CM000685.2:g.154969518C= | GRCh38 |
| NC_000023.10:g.154197793C= , CM000685.1:g.154197793C= | GRCh37 |
| NC_000023.9:g.153850987C= | NCBI36 |
| NG_011403.1:g.58206G= | |
| NG_011403.2:g.58206G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000132.4:c.822G= MANE Select | NP_000123.1:p.Trp274= |
| ENST00000360256.9:c.822G= MANE Select | ENSP00000353393.4:p.Trp274= |
| NM_000132.3:c.822G= | NP_000123.1:p.Trp274= |
| ENST00000360256.8:c.822G= | ENSP00000353393.4:p.Trp274= |
| ENST00000647125.1:c.*698G= | ENSP00000496062.1:n.*698G= |
| XM_011531126.1:c.717G= | XP_011529428.1:p.Trp239= |