Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2284280A>G , CM000678.2:g.2284280A>G | GRCh38 |
| NC_000016.9:g.2334281A>G , CM000678.1:g.2334281A>G | GRCh37 |
| NC_000016.8:g.2274282A>G | NCBI36 |
| NG_011790.1:g.61467T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001089.3:c.3861T>C MANE Select | NP_001080.2:p.Tyr1287= |
| ENST00000301732.10:c.3861T>C MANE Select | ENSP00000301732.5:p.Tyr1287= |
| NM_001089.2:c.3861T>C | NP_001080.2:p.Tyr1287= |
| ENST00000301732.9:c.3861T>C | ENSP00000301732.5:p.Tyr1287= |
| ENST00000382381.7:c.3687T>C | ENSP00000371818.3:p.Tyr1229= |