Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.84033413G>A , CM000678.2:g.84033413G>A | GRCh38 |
| NC_000016.9:g.84067018G>A , CM000678.1:g.84067018G>A | GRCh37 |
| NC_000016.8:g.82624519G>A | NCBI36 |
| NG_034136.1:g.13745C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001080442.3:c.445C>T MANE Select | NP_001073911.1:p.Gln149Ter |
| ENST00000299709.8:c.445C>T MANE Select | ENSP00000299709.3:p.Gln149Ter |
| NM_001080442.2:c.445C>T | NP_001073911.1:p.Gln149Ter |
| ENST00000299709.7:c.445C>T | ENSP00000299709.3:p.Gln149Ter |
| ENST00000568178.1:c.445C>T | ENSP00000457737.1:p.Gln149Ter |
| ENST00000569816.1:c.106C>T | ENSP00000455085.1:p.Gln36Ter |
| XM_011522872.1:c.445C>T | XP_011521174.1:p.Gln149Ter |
| XM_017022946.1:c.445C>T | XP_016878435.1:p.Gln149Ter |