Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.41348419A= , CM000681.2:g.41348419A= | GRCh38 |
| NC_000019.9:g.41854324A= , CM000681.1:g.41854324A= | GRCh37 |
| NC_000019.8:g.46546164A= | NCBI36 |
| NG_013364.1:g.10508T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221930.6:c.392T= MANE Select | ENSP00000221930.4:p.Ile131= | |
| ENST00000600196.2:c.392T= | ENSP00000504008.1:p.Ile131= | |
| ENST00000677934.1:c.392T= | ENSP00000504769.1:p.Ile131= | |
| ENST00000221930.5:c.392T= | ENSP00000221930.4:p.Ile131= | |
| NM_000660.5:c.392T= | NP_000651.3:p.Ile131= | |
| XM_011527242.1:c.392T= | XP_011525544.1:p.Ile131= | |
| NM_000660.6:c.392T= | NP_000651.3:p.Ile131= | |
| XM_011527242.2:c.392T= | XP_011525544.1:p.Ile131= | |
| NM_000660.7:c.392T= MANE Select | NP_000651.3:p.Ile131= |