Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.131890410G>T , CM000668.2:g.131890410G>T | GRCh38 |
| NC_000006.11:g.132211550G>T , CM000668.1:g.132211550G>T | GRCh37 |
| NC_000006.10:g.132253243G>T | NCBI36 |
| NG_008206.1:g.87395G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000684674.1:n.1108G>T | ||
| ENST00000647893.1:c.2677G>T MANE Select | ENSP00000498074.1:p.Glu893Ter | |
| ENST00000360971.6:c.2677G>T | ENSP00000354238.2:p.Glu893Ter | |
| ENST00000513998.5:c.*1514G>T | ENSP00000422424.1:n.*1514G>T | |
| NM_006208.2:c.2677G>T | NP_006199.2:p.Glu893Ter | |
| XM_011535896.1:c.1567G>T | XP_011534198.1:p.Glu523Ter | |
| NM_006208.3:c.2677G>T MANE Select | NP_006199.2:p.Glu893Ter |