Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.1474345G>C , CM000669.2:g.1474345G>C | GRCh38 |
| NC_000007.13:g.1513981G>C , CM000669.1:g.1513981G>C | GRCh37 |
| NC_000007.12:g.1480507G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000404767.8:c.5652C>G MANE Select | ENSP00000385722.3:p.Ile1884Met | |
| ENST00000404767.7:c.5652C>G | ENSP00000385722.3:p.Ile1884Met | |
| ENST00000482994.1:n.353C>G | ||
| NM_001080453.2:c.5652C>G | NP_001073922.2:p.Ile1884Met | |
| XM_011515260.1:c.5652C>G | XP_011513562.1:p.Ile1884Met | |
| XM_017011959.1:c.5652C>G | XP_016867448.1:p.Ile1884Met | |
| XM_017011960.1:c.5652C>G | XP_016867449.1:p.Ile1884Met | |
| NM_001080453.3:c.5652C>G MANE Select | NP_001073922.2:p.Ile1884Met |