Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.38071188A= , CM000664.2:g.38071188A= | GRCh38 |
| NC_000002.11:g.38298331A= , CM000664.1:g.38298331A= | GRCh37 |
| NC_000002.10:g.38151835A= | NCBI36 |
| NG_008386.2:g.9914T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000490576.2:c.1166T= | ENSP00000478839.2:p.Met389= | |
| ENST00000610745.5:c.1166T= MANE Select | ENSP00000478561.1:p.Met389= | |
| ENST00000492443.1:n.544T= | ||
| ENST00000494864.1:c.53T= | ENSP00000479876.1:p.Met18= | |
| ENST00000610745.4:c.1166T= | ENSP00000478561.1:p.Met389= | |
| ENST00000613082.1:n.561T= | ||
| ENST00000614273.1:c.1166T= | ENSP00000483678.1:p.Met389= | |
| NM_000104.3:c.1166T= | NP_000095.2:p.Met389= | |
| NM_000104.4:c.1166T= MANE Select | NP_000095.2:p.Met389= |