Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86643810C>T , CM000670.2:g.86643810C>T | GRCh38 |
| NC_000008.10:g.87656038C>T , CM000670.1:g.87656038C>T | GRCh37 |
| NC_000008.9:g.87725154C>T | NCBI36 |
| NG_016980.1:g.104866G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000320005.6:c.1119G>A MANE Select | ENSP00000316605.5:p.Trp373Ter | |
| ENST00000681546.1:n.939G>A | ||
| ENST00000681746.1:c.1119G>A | ENSP00000505959.1:p.Trp373Ter | |
| ENST00000320005.5:c.1119G>A | ENSP00000316605.5:p.Trp373Ter | |
| NM_019098.4:c.1119G>A | NP_061971.3:p.Trp373Ter | |
| XM_011517138.1:c.705G>A | XP_011515440.1:p.Trp235Ter | |
| XM_011517138.2:c.705G>A | XP_011515440.1:p.Trp235Ter | |
| NM_019098.5:c.1119G>A MANE Select | NP_061971.3:p.Trp373Ter |