Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.2787592A= , CM000686.2:g.2787592A= | GRCh38 |
| NC_000024.9:g.2655633A= , CM000686.1:g.2655633A= | GRCh37 |
| NC_000024.8:g.2715633A= | NCBI36 |
| NG_011751.1:g.5160T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003140.3:c.12T= MANE Select | NP_003131.1:p.Tyr4= |
| ENST00000383070.2:c.12T= MANE Select | ENSP00000372547.1:p.Tyr4= |
| NM_003140.2:c.12T= | NP_003131.1:p.Tyr4= |
| ENST00000383070.1:c.12T= | ENSP00000372547.1:p.Tyr4= |
| ENST00000679518.1:n.106+12853A= | |
| ENST00000680285.1:n.320-2157A= | |
| ENST00000680845.1:n.278A= | |
| ENST00000681787.1:n.106+12853A= | |
| ENST00000681940.1:n.106+12853A= |