Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.35310578C>T , CM000668.2:g.35310578C>T | GRCh38 |
| NC_000006.11:g.35278355C>T , CM000668.1:g.35278355C>T | GRCh37 |
| NC_000006.10:g.35386333C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000444278.3:c.246C>T | ENSP00000415357.3:p.Phe82= | |
| ENST00000698929.1:c.357C>T | ENSP00000514040.1:p.Phe119= | |
| ENST00000698930.1:c.357C>T | ENSP00000514041.1:p.Phe119= | |
| ENST00000698931.1:n.381C>T | ||
| ENST00000316637.7:c.357C>T MANE Select | ENSP00000319831.5:p.Phe119= | |
| ENST00000316637.6:c.357C>T | ENSP00000319831.5:p.Phe119= | |
| ENST00000444278.2:c.82C>T | ||
| NM_022047.3:c.357C>T | NP_071330.3:p.Phe119= | |
| NM_022047.4:c.357C>T MANE Select | NP_071330.3:p.Phe119= |