Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44351774G= , CM000679.2:g.44351774G= | GRCh38 |
| NC_000017.10:g.42429142G= , CM000679.1:g.42429142G= | GRCh37 |
| NC_000017.9:g.39784668G= | NCBI36 |
| NG_007886.1:g.11652G= , LRG_661:g.11652G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000053867.8:c.1158G= MANE Select | ENSP00000053867.2:p.Trp386= | |
| ENST00000639447.1:c.1136+22G= | ENSP00000492014.1:n.1136+22G= | |
| ENST00000053867.7:c.1158G= | ENSP00000053867.2:p.Trp386= | |
| ENST00000586443.1:c.599G= | ||
| ENST00000589265.5:c.687G= | ENSP00000467616.1:p.Trp229= | |
| ENST00000589923.1:n.416G= | ||
| NM_002087.3:c.1158G= | NP_002078.1:p.Trp386= | |
| XM_005257253.1:c.1158G= | XP_005257310.1:p.Trp386= | |
| XM_024450730.1:c.1158G= | XP_024306498.1:p.Trp386= | |
| NM_002087.4:c.1158G= MANE Select | NP_002078.1:p.Trp386= |