Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.86030357T>C , CM000664.2:g.86030357T>C | GRCh38 |
| NC_000002.11:g.86257480T>C , CM000664.1:g.86257480T>C | GRCh37 |
| NC_000002.10:g.86110991T>C | NCBI36 |
| NG_050742.2:g.80799A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263857.11:c.4618A>G MANE Select | ENSP00000263857.6:p.Met1540Val | |
| ENST00000263857.10:c.4618A>G | ENSP00000263857.6:p.Met1540Val | |
| ENST00000409681.1:c.4435A>G | ENSP00000386300.1:p.Met1479Val | |
| NM_015425.3:c.4618A>G | NP_056240.2:p.Met1540Val | |
| XM_006711983.2:c.4294A>G | XP_006712046.1:p.Met1432Val | |
| NM_015425.5:c.4618A>G | NP_056240.2:p.Met1540Val | |
| NM_015425.6:c.4618A>G MANE Select | NP_056240.2:p.Met1540Val |