Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.147132460T= , CM000669.2:g.147132460T= | GRCh38 |
| NC_000007.13:g.146829552T= , CM000669.1:g.146829552T= | GRCh37 |
| NC_000007.12:g.146460485T= | NCBI36 |
| NG_007092.2:g.1021100T= | |
| NG_007092.3:g.1021460T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361727.8:c.1299T= MANE Select | ENSP00000354778.3:p.Val433= | |
| ENST00000636561.1:n.1202T= | ||
| ENST00000636870.1:n.1161T= | ||
| ENST00000637150.1:n.1228T= | ||
| ENST00000637694.1:n.1202T= | ||
| ENST00000637825.1:n.782T= | ||
| ENST00000638117.1:n.1202T= | ||
| ENST00000361727.7:c.1299T= | ENSP00000354778.3:p.Val433= | |
| NM_014141.5:c.1299T= | NP_054860.1:p.Val433= | |
| XM_017011950.2:c.1299T= | XP_016867439.1:p.Val433= | |
| NM_014141.6:c.1299T= MANE Select | NP_054860.1:p.Val433= |