Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7529159G= , CM000681.2:g.7529159G= | GRCh38 |
| NC_000019.9:g.7594045G= , CM000681.1:g.7594045G= | GRCh37 |
| NC_000019.8:g.7500045G= | NCBI36 |
| NG_013374.1:g.8G= | |
| NG_015806.1:g.11550G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.1193G= MANE Select | ENSP00000264079.5:p.Trp398= | |
| ENST00000264079.10:c.1193G= | ENSP00000264079.5:p.Trp398= | |
| ENST00000394321.9:n.1508G= | ||
| ENST00000594692.1:n.189G= | ||
| ENST00000595860.5:n.376G= | ||
| ENST00000599334.1:c.70G= | ||
| NM_020533.2:c.1193G= | NP_065394.1:p.Trp398= | |
| NM_020533.3:c.1193G= MANE Select | NP_065394.1:p.Trp398= |