Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31270269T= , CM000668.2:g.31270269T= | GRCh38 |
| NC_000006.11:g.31238046T= , CM000668.1:g.31238046T= | GRCh37 |
| NC_000006.10:g.31346025T= | NCBI36 |
| NG_029422.2:g.6863A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000376228.10:c.836A= MANE Select | ENSP00000365402.5:p.Gln279= | |
| ENST00000376228.9:c.836A= | ENSP00000365402.5:p.Gln279= | |
| ENST00000376237.8:c.*423A= | ENSP00000365412.4:n.*423A= | |
| ENST00000383329.7:c.836A= | ENSP00000372819.3:p.Gln279= | |
| ENST00000415537.1:c.727A= | ||
| ENST00000470363.5:n.154A= | ||
| ENST00000487245.5:n.1195A= | ||
| ENST00000495835.1:n.1025A= | ||
| NM_002117.5:c.836A= | NP_002108.4:p.Gln279= | |
| NM_002117.6:c.836A= MANE Select | NP_002108.4:p.Gln279= |