Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.35437905A= , CM000682.2:g.35437905A= | GRCh38 |
| NC_000020.10:g.34025685A= , CM000682.1:g.34025685A= | GRCh37 |
| NC_000020.9:g.33489099A= | NCBI36 |
| NG_008076.2:g.5315T= | |
| NG_008076.3:g.21842T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374369.8:c.24T= MANE Select | ENSP00000363489.3:p.Thr8= | |
| ENST00000374369.7:c.24T= | ENSP00000363489.3:p.Thr8= | |
| ENST00000374372.1:c.24T= | ENSP00000363492.1:p.Thr8= | |
| NM_000557.4:c.24T= | NP_000548.2:p.Thr8= | |
| XM_011529075.1:c.24T= | XP_011527377.1:p.Thr8= | |
| XM_011529076.1:c.24T= | XP_011527378.1:p.Thr8= | |
| NM_001319138.1:c.24T= | NP_001306067.1:p.Thr8= | |
| NM_000557.5:c.24T= MANE Select | NP_000548.2:p.Thr8= | |
| NM_001319138.2:c.24T= | NP_001306067.1:p.Thr8= |