Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118312799T= , CM000673.2:g.118312799T= | GRCh38 |
| NC_000011.9:g.118183514T= , CM000673.1:g.118183514T= | GRCh37 |
| NC_000011.8:g.117688724T= | NCBI36 |
| NG_007383.1:g.13220T= , LRG_38:g.13220T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361763.9:c.285T= MANE Select | ENSP00000354566.4:p.Tyr95= | |
| ENST00000361763.8:c.285T= | ENSP00000354566.4:p.Tyr95= | |
| ENST00000526146.5:n.831T= | ||
| ENST00000528435.5:n.838T= | ||
| ENST00000528600.1:c.267T= | ENSP00000433975.1:p.Tyr89= | |
| ENST00000529713.5:n.391T= | ||
| ENST00000531913.1:n.656T= | ||
| NM_000733.3:c.285T= , LRG_38t1:c.285T= | NP_000724.1:p.Tyr95= | |
| NM_000733.4:c.285T= MANE Select | NP_000724.1:p.Tyr95= |