Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.77518121C>A , CM000676.2:g.77518121C>A | GRCh38 |
| NC_000014.8:g.77984464C>A , CM000676.1:g.77984464C>A | GRCh37 |
| NC_000014.7:g.77054217C>A | NCBI36 |
| NG_028282.1:g.103647G>T , LRG_371:g.103647G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000686627.1:n.518G>T | ||
| ENST00000687688.1:n.1249G>T | ||
| ENST00000692906.1:n.1218G>T | ||
| ENST00000216484.7:c.1486G>T MANE Select | ENSP00000216484.2:p.Val496Phe | |
| ENST00000216484.6:c.1486G>T | ENSP00000216484.2:p.Val496Phe | |
| ENST00000556607.1:c.314G>T | ENSP00000451029.1:n.314G>T | |
| NM_004863.3:c.1486G>T , LRG_371t1:c.1486G>T | NP_004854.1:p.Val496Phe | |
| NM_004863.4:c.1486G>T MANE Select | NP_004854.1:p.Val496Phe |