Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67436096G>A , CM000678.2:g.67436096G>A | GRCh38 |
| NC_000016.9:g.67469999G>A , CM000678.1:g.67469999G>A | GRCh37 |
| NC_000016.8:g.66027500G>A | NCBI36 |
| NG_011482.1:g.50091C>T | |
| NG_016549.1:g.9964G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326152.6:c.618G>A MANE Select | ENSP00000316786.5:p.Leu206= | |
| ENST00000326152.5:c.618G>A | ENSP00000316786.5:p.Leu206= | |
| ENST00000566606.1:c.596G>A | ENSP00000473429.1:n.596G>A | |
| ENST00000567684.2:n.481G>A | ||
| NM_000196.3:c.618G>A | NP_000187.3:p.Leu206= | |
| NM_000196.4:c.618G>A MANE Select | NP_000187.3:p.Leu206= |