Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.74774641A>G , CM000678.2:g.74774641A>G | GRCh38 |
| NC_000016.9:g.74808539A>G , CM000678.1:g.74808539A>G | GRCh37 |
| NC_000016.8:g.73366040A>G | NCBI36 |
| NG_017070.1:g.5191T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_024306.5:c.115T>C MANE Select | NP_077282.3:p.Phe39Leu |
| ENST00000219368.8:c.115T>C MANE Select | ENSP00000219368.3:p.Phe39Leu |
| NM_024306.4:c.115T>C | NP_077282.3:p.Phe39Leu |
| ENST00000219368.7:c.115T>C | ENSP00000219368.3:p.Phe39Leu |
| ENST00000567683.5:c.115T>C | ENSP00000455126.1:p.Phe39Leu |
| XM_011523317.1:c.115T>C | XP_011521619.1:p.Phe39Leu |
| XM_011523317.3:c.115T>C | XP_011521619.1:p.Phe39Leu |
| XM_011523318.1:c.115T>C | XP_011521620.1:p.Phe39Leu |