Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.2787113T= , CM000686.2:g.2787113T= | GRCh38 |
| NC_000024.9:g.2655154T= , CM000686.1:g.2655154T= | GRCh37 |
| NC_000024.8:g.2715154T= | NCBI36 |
| NG_011751.1:g.5639A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000679518.1:n.106+12374T= | ||
| ENST00000679825.1:n.225T= | ||
| ENST00000680285.1:n.320-2636T= | ||
| ENST00000680845.1:n.165+60T= | ||
| ENST00000681787.1:n.106+12374T= | ||
| ENST00000681940.1:n.106+12374T= | ||
| ENST00000383070.2:c.491A= MANE Select | ENSP00000372547.1:p.Tyr164= | |
| ENST00000383070.1:c.491A= | ENSP00000372547.1:p.Tyr164= | |
| NM_003140.2:c.491A= | NP_003131.1:p.Tyr164= | |
| NM_003140.3:c.491A= MANE Select | NP_003131.1:p.Tyr164= |