Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94007577A>G , CM000663.2:g.94007577A>G | GRCh38 |
| NC_000001.10:g.94473133A>G , CM000663.1:g.94473133A>G | GRCh37 |
| NC_000001.9:g.94245721A>G | NCBI36 |
| NG_009073.1:g.118573T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.6005+57T>C MANE Select | ENSP00000359245.3:n.6005+57T>C | |
| ENST00000370225.3:c.6005+57T>C | ENSP00000359245.3:n.6005+57T>C | |
| ENST00000465352.1:n.421+57T>C | ||
| ENST00000484388.1:n.119+57T>C | ||
| ENST00000536513.5:c.2381+57T>C | ENSP00000439707.2:n.2381+57T>C | |
| NM_000350.2:c.6005+57T>C | NP_000341.2:n.6005+57T>C | |
| NM_000350.3:c.6005+57T>C MANE Select | NP_000341.2:n.6005+57T>C |