Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1985905C>G , CM000678.2:g.1985905C>G | GRCh38 |
| NC_000016.9:g.2035906C>G , CM000678.1:g.2035906C>G | GRCh37 |
| NC_000016.8:g.1975907C>G | NCBI36 |
| NG_016288.1:g.6757C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000567719.2:c.270C>G | ENSP00000455885.1:p.Cys90Trp | |
| ENST00000248114.7:c.495C>G MANE Select | ENSP00000248114.6:p.Cys165Trp | |
| ENST00000248114.6:c.495C>G | ENSP00000248114.6:p.Cys165Trp | |
| ENST00000565658.1:n.652C>G | ||
| ENST00000567719.1:c.270C>G | ENSP00000455885.1:p.Cys90Trp | |
| ENST00000569451.1:c.298C>G | ENSP00000456432.1:p.Leu100Val | |
| NM_005262.2:c.495C>G | NP_005253.3:p.Cys165Trp | |
| NM_005262.3:c.495C>G MANE Select | NP_005253.3:p.Cys165Trp |