Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218893209T= , CM000664.2:g.218893209T= | GRCh38 |
| NC_000002.11:g.219757931T= , CM000664.1:g.219757931T= | GRCh37 |
| NC_000002.10:g.219466175T= | NCBI36 |
| NG_012179.1:g.17677T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258411.8:c.1192T= MANE Select | ENSP00000258411.3:p.Trp398= | |
| ENST00000258411.7:c.1192T= | ENSP00000258411.3:p.Trp398= | |
| NM_025216.2:c.1192T= | NP_079492.2:p.Trp398= | |
| XM_011511928.1:c.1141T= | XP_011510230.1:p.Trp381= | |
| XM_011511929.1:c.1096T= | XP_011510231.1:p.Trp366= | |
| XM_011511930.1:c.812T= | XP_011510232.1:p.Leu271= | |
| XM_011511929.2:c.1096T= | XP_011510231.1:p.Trp366= | |
| NM_025216.3:c.1192T= MANE Select | NP_079492.2:p.Trp398= |