Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.69353154G>A , CM000674.2:g.69353154G>A | GRCh38 |
| NC_000012.11:g.69746934G>A , CM000674.1:g.69746934G>A | GRCh37 |
| NC_000012.10:g.68033201G>A | NCBI36 |
| NG_008195.1:g.9801G>A , LRG_768:g.9801G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261267.7:c.382G>A MANE Select | ENSP00000261267.2:p.Val128Met | |
| ENST00000261267.6:c.382G>A | ENSP00000261267.2:p.Val128Met | |
| ENST00000549690.1:c.303G>A | ENSP00000449898.1:p.Gly101= | |
| NM_000239.2:c.382G>A , LRG_768t1:c.382G>A | NP_000230.1:p.Val128Met | |
| NM_000239.3:c.382G>A MANE Select | NP_000230.1:p.Val128Met |