Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.93998092G>A , CM000663.2:g.93998092G>A | GRCh38 |
| NC_000001.10:g.94463648G>A , CM000663.1:g.94463648G>A | GRCh37 |
| NC_000001.9:g.94236236G>A | NCBI36 |
| NG_009073.1:g.128058C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.6498C>T MANE Select | ENSP00000359245.3:p.Ile2166= | |
| ENST00000370225.3:c.6498C>T | ENSP00000359245.3:p.Ile2166= | |
| ENST00000536513.5:c.2874C>T | ENSP00000439707.2:p.Ile958= | |
| NM_000350.2:c.6498C>T | NP_000341.2:p.Ile2166= | |
| NM_000350.3:c.6498C>T MANE Select | NP_000341.2:p.Ile2166= |