Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.47582461A= , CM000673.2:g.47582461A= | GRCh38 |
| NC_000011.9:g.47604013A= , CM000673.1:g.47604013A= | GRCh37 |
| NC_000011.8:g.47560589A= | NCBI36 |
| NG_011946.1:g.8452A= | |
| NG_011946.2:g.8452A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263774.9:c.620A= MANE Select | ENSP00000263774.4:p.Tyr207= | |
| ENST00000531351.2:n.1815A= | ||
| ENST00000677462.1:n.3094A= | ||
| ENST00000678975.1:n.2877A= | ||
| ENST00000263774.8:c.620A= | ENSP00000263774.4:p.Tyr207= | |
| ENST00000524568.1:n.723A= | ||
| ENST00000525212.1:n.275A= | ||
| ENST00000525378.5:n.558A= | ||
| ENST00000527178.1:n.220A= | ||
| ENST00000533507.5:n.1514A= | ||
| NM_004551.2:c.620A= | NP_004542.1:p.Tyr207= | |
| NM_004551.3:c.620A= MANE Select | NP_004542.1:p.Tyr207= |