Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2281064A>G , CM000678.2:g.2281064A>G | GRCh38 |
| NC_000016.9:g.2331065A>G , CM000678.1:g.2331065A>G | GRCh37 |
| NC_000016.8:g.2271066A>G | NCBI36 |
| NG_011790.1:g.64683T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301732.10:c.4322T>C MANE Select | ENSP00000301732.5:p.Phe1441Ser | |
| ENST00000301732.9:c.4322T>C | ENSP00000301732.5:p.Phe1441Ser | |
| ENST00000382381.7:c.4148T>C | ENSP00000371818.3:p.Phe1383Ser | |
| ENST00000566200.1:n.843T>C | ||
| NM_001089.2:c.4322T>C | NP_001080.2:p.Phe1441Ser | |
| NM_001089.3:c.4322T>C MANE Select | NP_001080.2:p.Phe1441Ser |