Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31270367C= , CM000668.2:g.31270367C= | GRCh38 |
| NC_000006.11:g.31238144C= , CM000668.1:g.31238144C= | GRCh37 |
| NC_000006.10:g.31346123C= | NCBI36 |
| NG_029422.2:g.6765G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.738G= MANE Select | ENSP00000365402.5:p.Glu246= | |
| ENST00000376228.9:c.738G= | ENSP00000365402.5:p.Glu246= | |
| ENST00000376237.8:c.*325G= | ENSP00000365412.4:n.*325G= | |
| ENST00000383329.7:c.738G= | ENSP00000372819.3:p.Glu246= | |
| ENST00000415537.1:c.665-36G= | ||
| ENST00000470363.5:n.56G= | ||
| ENST00000487245.5:n.1097G= | ||
| ENST00000495835.1:n.927G= | ||
| NM_002117.5:c.738G= | NP_002108.4:p.Glu246= | |
| NM_002117.6:c.738G= MANE Select | NP_002108.4:p.Glu246= |