Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.110169643A>C , CM000675.2:g.110169643A>C | GRCh38 |
| NC_000013.10:g.110821990A>C , CM000675.1:g.110821990A>C | GRCh37 |
| NC_000013.9:g.109619991A>C | NCBI36 |
| NG_011544.2:g.142507T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375820.10:c.3862T>G MANE Select | ENSP00000364979.4:p.Phe1288Val | |
| ENST00000650424.1:c.18T>G | ||
| ENST00000375820.8:c.3862T>G | ENSP00000364979.4:p.Phe1288Val | |
| NM_001845.5:c.3862T>G | NP_001836.3:p.Phe1288Val | |
| XM_011521048.1:c.3670T>G | XP_011519350.1:p.Phe1224Val | |
| XM_011521048.2:c.3670T>G | XP_011519350.1:p.Phe1224Val | |
| NM_001845.6:c.3862T>G MANE Select | NP_001836.3:p.Phe1288Val |