Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.91272650A= , CM000676.2:g.91272650A= | GRCh38 |
| NC_000014.8:g.91738994A= , CM000676.1:g.91738994A= | GRCh37 |
| NC_000014.7:g.90808747A= | NCBI36 |
| NG_033118.1:g.150195T= | |
| NG_033118.2:g.150195T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389857.11:c.6062T= MANE Select | ENSP00000374507.6:p.Val2021= | |
| ENST00000331194.8:c.1496T= | ENSP00000330332.8:p.Val499= | |
| ENST00000389857.10:c.6062T= | ENSP00000374507.6:p.Val2021= | |
| ENST00000556726.5:c.2290T= | ||
| NM_001080414.3:c.6062T= | NP_001073883.2:p.Val2021= | |
| XM_011536796.1:c.5954T= | XP_011535098.1:p.Val1985= | |
| XM_011536796.2:c.5954T= | XP_011535098.1:p.Val1985= | |
| XM_017021336.1:c.3143T= | XP_016876825.1:p.Val1048= | |
| NM_001080414.4:c.6062T= MANE Select | NP_001073883.2:p.Val2021= |