Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118312802T>A , CM000673.2:g.118312802T>A | GRCh38 |
| NC_000011.9:g.118183517T>A , CM000673.1:g.118183517T>A | GRCh37 |
| NC_000011.8:g.117688727T>A | NCBI36 |
| NG_007383.1:g.13223T>A , LRG_38:g.13223T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000733.4:c.288T>A MANE Select | NP_000724.1:p.Tyr96Ter |
| ENST00000361763.9:c.288T>A MANE Select | ENSP00000354566.4:p.Tyr96Ter |
| NM_000733.3:c.288T>A , LRG_38t1:c.288T>A | NP_000724.1:p.Tyr96Ter |
| ENST00000361763.8:c.288T>A | ENSP00000354566.4:p.Tyr96Ter |
| ENST00000526146.5:n.834T>A | |
| ENST00000528435.5:n.841T>A | |
| ENST00000528600.1:c.270T>A | ENSP00000433975.1:p.Tyr90Ter |
| ENST00000529713.5:n.394T>A | |
| ENST00000531913.1:n.659T>A |