Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.38253186A= , CM000677.2:g.38253186A= | GRCh38 |
| NC_000015.9:g.38545387A= , CM000677.1:g.38545387A= | GRCh37 |
| NC_000015.8:g.36332679A= | NCBI36 |
| NG_008980.1:g.5336A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299084.9:c.1A= MANE Select | ENSP00000299084.4:p.Met1= | |
| ENST00000299084.8:c.1A= | ENSP00000299084.4:p.Met1= | |
| ENST00000561205.1:n.339A= | ||
| ENST00000561317.1:c.-127A= | ENSP00000453680.1:n.-127A= | |
| NM_152594.2:c.1A= | NP_689807.1:p.Met1= | |
| XM_005254202.2:c.1A= | XP_005254259.1:p.Met1= | |
| XM_005254203.3:c.-47A= | XP_005254260.1:n.-47A= | |
| XM_005254202.3:c.1A= | XP_005254259.1:p.Met1= | |
| XR_001751484.1:n.87+381T= | ||
| NM_152594.3:c.1A= MANE Select | NP_689807.1:p.Met1= |