Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.93218697G>C , CM000676.2:g.93218697G>C | GRCh38 |
| NC_000014.8:g.93685043G>C , CM000676.1:g.93685043G>C | GRCh37 |
| NC_000014.7:g.92754796G>C | NCBI36 |
| NG_051089.1:g.16642G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000013070.11:c.772G>C MANE Select | ENSP00000013070.6:p.Glu258Gln | |
| ENST00000013070.10:c.772G>C | ENSP00000013070.6:p.Glu258Gln | |
| ENST00000416753.5:c.544G>C | ENSP00000391706.2:p.Glu182Gln | |
| ENST00000553674.1:c.*473G>C | ENSP00000450470.1:n.*473G>C | |
| ENST00000553857.5:c.378+3416G>C | ||
| ENST00000555329.1:c.17G>C | ||
| NM_175748.3:c.772G>C | NP_786924.2:p.Glu258Gln | |
| NR_038150.1:n.874G>C | ||
| NM_175748.4:c.772G>C MANE Select | NP_786924.2:p.Glu258Gln | |
| NR_038150.2:n.674G>C |