Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.6778284C= , CM000682.2:g.6778284C= | GRCh38 |
| NC_000020.10:g.6758931C= , CM000682.1:g.6758931C= | GRCh37 |
| NC_000020.9:g.6706931C= | NCBI36 |
| NG_023233.1:g.15187C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378827.5:c.386C= MANE Select | ENSP00000368104.3:p.Thr129= | |
| ENST00000378827.4:c.386C= | ENSP00000368104.3:p.Thr129= | |
| NM_001200.2:c.386C= | NP_001191.1:p.Thr129= | |
| XM_011529323.1:c.-83C= | XP_011527625.1:n.-83C= | |
| NM_001200.3:c.386C= | NP_001191.1:p.Thr129= | |
| NM_001200.4:c.386C= MANE Select | NP_001191.1:p.Thr129= |