Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10658619A= , CM000682.2:g.10658619A= | GRCh38 |
| NC_000020.10:g.10639267A= , CM000682.1:g.10639267A= | GRCh37 |
| NC_000020.9:g.10587267A= | NCBI36 |
| NG_007496.1:g.20428T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000214.3:c.543T= MANE Select | NP_000205.1:p.Tyr181= |
| ENST00000254958.10:c.543T= MANE Select | ENSP00000254958.4:p.Tyr181= |
| NM_000214.2:c.543T= | NP_000205.1:p.Tyr181= |
| ENST00000254958.9:c.543T= | ENSP00000254958.4:p.Tyr181= |
| ENST00000423891.6:n.409T= |