Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118312796T= , CM000673.2:g.118312796T= | GRCh38 |
| NC_000011.9:g.118183511T= , CM000673.1:g.118183511T= | GRCh37 |
| NC_000011.8:g.117688721T= | NCBI36 |
| NG_007383.1:g.13217T= , LRG_38:g.13217T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361763.9:c.282T= MANE Select | ENSP00000354566.4:p.Gly94= | |
| ENST00000361763.8:c.282T= | ENSP00000354566.4:p.Gly94= | |
| ENST00000526146.5:n.828T= | ||
| ENST00000528435.5:n.835T= | ||
| ENST00000528600.1:c.264T= | ENSP00000433975.1:p.Gly88= | |
| ENST00000529713.5:n.388T= | ||
| ENST00000531913.1:n.653T= | ||
| NM_000733.3:c.282T= , LRG_38t1:c.282T= | NP_000724.1:p.Gly94= | |
| NM_000733.4:c.282T= MANE Select | NP_000724.1:p.Gly94= |