Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.107947417C>T , CM000666.2:g.107947417C>T | GRCh38 |
| NC_000004.11:g.108868573C>T , CM000666.1:g.108868573C>T | GRCh37 |
| NC_000004.10:g.109088022C>T | NCBI36 |
| NG_007961.1:g.20857C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_183075.3:c.1168C>T MANE Select | NP_898898.1:p.Arg390Ter |
| ENST00000332884.11:c.1168C>T MANE Select | ENSP00000333212.6:p.Arg390Ter |
| NM_183075.2:c.1168C>T | NP_898898.1:p.Arg390Ter |
| ENST00000332884.10:c.1168C>T | ENSP00000333212.6:p.Arg390Ter |
| ENST00000508453.1:c.541C>T | ENSP00000423667.1:p.Arg181Ter |
| XM_005262717.2:c.1222C>T | XP_005262774.1:p.Arg408Ter |
| XM_005262720.2:c.532C>T | XP_005262777.1:p.Arg178Ter |
| XR_001741783.1:n.156-36868G>A | |
| XR_001741784.1:n.530+31303G>A |