Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.84016607C>A , CM000678.2:g.84016607C>A | GRCh38 |
| NC_000016.9:g.84050212C>A , CM000678.1:g.84050212C>A | GRCh37 |
| NC_000016.8:g.82607713C>A | NCBI36 |
| NG_034136.1:g.30551G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001080442.3:c.1074G>T MANE Select | NP_001073911.1:p.Thr358= |
| ENST00000299709.8:c.1074G>T MANE Select | ENSP00000299709.3:p.Thr358= |
| NM_001080442.2:c.1074G>T | NP_001073911.1:p.Thr358= |
| ENST00000299709.7:c.1074G>T | ENSP00000299709.3:p.Thr358= |
| ENST00000568003.1:n.150G>T | |
| XM_011522872.1:c.1074G>T | XP_011521174.1:p.Thr358= |
| XM_017022946.1:c.1074G>T | XP_016878435.1:p.Thr358= |