Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.144397441A>G , CM000669.2:g.144397441A>G | GRCh38 |
| NC_000007.13:g.144094534A>G , CM000669.1:g.144094534A>G | GRCh37 |
| NC_000007.12:g.143725467A>G | NCBI36 |
| NG_028979.1:g.17787T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645489.1:c.1524T>C | ENSP00000496732.1:p.Phe508= | |
| ENST00000467773.1:c.1875T>C MANE Select | ENSP00000419457.1:p.Phe625= | |
| ENST00000483238.5:c.1779T>C | ENSP00000419565.1:p.Phe593= | |
| NM_001080413.3:c.1875T>C MANE Select | NP_001073882.3:p.Phe625= | |
| XM_011515791.1:c.1524T>C | XP_011514093.1:p.Phe508= | |
| XM_017011742.2:c.1779T>C | XP_016867231.1:p.Phe593= |