Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63941169A>G , CM000679.2:g.63941169A>G | GRCh38 |
| NC_000017.10:g.62018529A>G , CM000679.1:g.62018529A>G | GRCh37 |
| NC_000017.9:g.59372261A>G | NCBI36 |
| NG_011699.1:g.36750T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000334.4:c.5113T>C MANE Select | NP_000325.4:p.Phe1705Leu |
| ENST00000435607.3:c.5113T>C MANE Select | ENSP00000396320.1:p.Phe1705Leu |
| ENST00000578147.5:c.5113T>C | ENSP00000463963.1:p.Phe1705Leu |
| XM_005257566.3:c.5113T>C | XP_005257623.1:p.Phe1705Leu |