Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67585227A= , CM000673.2:g.67585227A= | GRCh38 |
| NC_000011.9:g.67352698A= , CM000673.1:g.67352698A= | GRCh37 |
| NC_000011.8:g.67109274A= | NCBI36 |
| NG_012075.1:g.6633A= , LRG_723:g.6633A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000398603.6:c.322A= | ENSP00000381604.1:p.Ile108= | |
| ENST00000398606.10:c.322A= MANE Select | ENSP00000381607.3:p.Ile108= | |
| ENST00000646888.1:c.*38A= | ENSP00000494477.1:n.*38A= | |
| ENST00000398603.5:c.322A= | ENSP00000381604.1:p.Ile108= | |
| ENST00000398606.7:c.322A= | ENSP00000381607.3:p.Ile108= | |
| ENST00000467591.1:n.433A= | ||
| ENST00000494593.1:n.1117A= | ||
| ENST00000498765.5:c.385A= | ||
| NM_000852.3:c.322A= , LRG_723t1:c.322A= | NP_000843.1:p.Ile108= | |
| NM_000852.4:c.322A= MANE Select | NP_000843.1:p.Ile108= |