Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.17068723G>T , CM000672.2:g.17068723G>T | GRCh38 |
| NC_000010.10:g.17110722G>T , CM000672.1:g.17110722G>T | GRCh37 |
| NC_000010.9:g.17150728G>T | NCBI36 |
| NG_008967.1:g.66095C>A , LRG_540:g.66095C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000377833.10:c.2673C>A MANE Select | ENSP00000367064.4:p.Cys891Ter | |
| ENST00000377833.8:c.2673C>A | ENSP00000367064.4:p.Cys891Ter | |
| NM_001081.3:c.2673C>A , LRG_540t1:c.2673C>A | NP_001072.2:p.Cys891Ter | |
| XM_011519708.1:c.2673C>A | XP_011518010.1:p.Cys891Ter | |
| XM_011519708.2:c.2673C>A | XP_011518010.1:p.Cys891Ter | |
| NM_001081.4:c.2673C>A MANE Select | NP_001072.2:p.Cys891Ter |