Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.89210140A= , CM000677.2:g.89210140A= | GRCh38 |
| NC_000015.9:g.89753371A= , CM000677.1:g.89753371A= | GRCh37 |
| NC_000015.8:g.87554375A= | NCBI36 |
| NG_008116.1:g.16552T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000268125.10:c.*145T= MANE Select | ENSP00000268125.5:n.*145T= | |
| ENST00000268125.9:c.*145T= | ENSP00000268125.5:n.*145T= | |
| ENST00000563254.1:c.471T= | ||
| NM_000326.4:c.*145T= | NP_000317.1:n.*145T= | |
| XM_011521870.1:c.*145T= | XP_011520172.1:n.*145T= | |
| XM_011521871.1:c.*145T= | XP_011520173.1:n.*145T= | |
| XM_011521872.1:c.*145T= | XP_011520174.1:n.*145T= | |
| XM_011521870.2:c.*145T= | XP_011520172.1:n.*145T= | |
| XM_017022460.1:c.*145T= | XP_016877949.1:n.*145T= | |
| NM_000326.5:c.*145T= MANE Select | NP_000317.1:n.*145T= |