Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86575947C>A , CM000670.2:g.86575947C>A | GRCh38 |
| NC_000008.10:g.87588175C>A , CM000670.1:g.87588175C>A | GRCh37 |
| NC_000008.9:g.87657291C>A | NCBI36 |
| NG_016980.1:g.172729G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.2287G>T MANE Select | ENSP00000316605.5:p.Val763Leu | |
| ENST00000681546.1:n.2107G>T | ||
| ENST00000681746.1:c.*698G>T | ENSP00000505959.1:n.*698G>T | |
| ENST00000320005.5:c.2287G>T | ENSP00000316605.5:p.Val763Leu | |
| ENST00000517327.5:c.276+2742G>T | ENSP00000428329.1:n.276+2742G>T | |
| NM_019098.4:c.2287G>T | NP_061971.3:p.Val763Leu | |
| XM_011517138.1:c.1873G>T | XP_011515440.1:p.Val625Leu | |
| XM_011517138.2:c.1873G>T | XP_011515440.1:p.Val625Leu | |
| NM_019098.5:c.2287G>T MANE Select | NP_061971.3:p.Val763Leu |