Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.16132115A>G , CM000663.2:g.16132115A>G | GRCh38 |
| NC_000001.10:g.16458610A>G , CM000663.1:g.16458610A>G | GRCh37 |
| NC_000001.9:g.16331197A>G | NCBI36 |
| NG_021396.1:g.28973T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358432.8:c.2274T>C MANE Select | ENSP00000351209.5:p.Phe758= | |
| ENST00000358432.7:c.2274T>C | ENSP00000351209.5:p.Phe758= | |
| NM_004431.3:c.2274T>C | NP_004422.2:p.Phe758= | |
| NM_001329090.1:c.2112T>C | NP_001316019.1:p.Phe704= | |
| NM_004431.4:c.2274T>C | NP_004422.2:p.Phe758= | |
| NM_004431.5:c.2274T>C MANE Select | NP_004422.2:p.Phe758= | |
| NM_001329090.2:c.2112T>C | NP_001316019.1:p.Phe704= |