Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94056626A>G , CM000663.2:g.94056626A>G | GRCh38 |
| NC_000001.10:g.94522182A>G , CM000663.1:g.94522182A>G | GRCh37 |
| NC_000001.9:g.94294770A>G | NCBI36 |
| NG_009073.1:g.69524T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.2357T>C MANE Select | ENSP00000359245.3:p.Met786Thr | |
| ENST00000649773.1:c.2161-1311T>C | ENSP00000496882.1:n.2161-1311T>C | |
| ENST00000370225.3:c.2357T>C | ENSP00000359245.3:p.Met786Thr | |
| ENST00000536513.5:c.-65+6548T>C | ENSP00000439707.2:n.-65+6548T>C | |
| NM_000350.2:c.2357T>C | NP_000341.2:p.Met786Thr | |
| NM_000350.3:c.2357T>C MANE Select | NP_000341.2:p.Met786Thr |