Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48364952C>T , CM000675.2:g.48364952C>T | GRCh38 |
| NC_000013.10:g.48939088C>T , CM000675.1:g.48939088C>T | GRCh37 |
| NC_000013.9:g.47837089C>T | NCBI36 |
| NG_009009.1:g.66206C>T , LRG_517:g.66206C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000321.3:c.920C>T MANE Select | NP_000312.2:p.Thr307Ile |
| ENST00000267163.6:c.920C>T MANE Select | ENSP00000267163.4:p.Thr307Ile |
| NM_000321.2:c.920C>T , LRG_517t1:c.920C>T | NP_000312.2:p.Thr307Ile |
| ENST00000267163.4:c.920C>T | ENSP00000267163.4:p.Thr307Ile |
| ENST00000650461.1:c.920C>T | ENSP00000497193.1:p.Thr307Ile |
| XM_011535171.1:c.659C>T | XP_011533473.1:p.Thr220Ile |
| XM_011535171.2:c.659C>T | XP_011533473.1:p.Thr220Ile |
| XR_002957522.1:n.146G>A |