Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94001967A>T , CM000663.2:g.94001967A>T | GRCh38 |
| NC_000001.10:g.94467523A>T , CM000663.1:g.94467523A>T | GRCh37 |
| NC_000001.9:g.94240111A>T | NCBI36 |
| NG_009073.1:g.124183T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.6173T>A MANE Select | ENSP00000359245.3:p.Leu2058Gln | |
| ENST00000370225.3:c.6173T>A | ENSP00000359245.3:p.Leu2058Gln | |
| ENST00000465352.1:n.589T>A | ||
| ENST00000536513.5:c.2549T>A | ENSP00000439707.2:p.Leu850Gln | |
| NM_000350.2:c.6173T>A | NP_000341.2:p.Leu2058Gln | |
| NM_000350.3:c.6173T>A MANE Select | NP_000341.2:p.Leu2058Gln |