Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.45108841C>A , CM000677.2:g.45108841C>A | GRCh38 |
| NC_000015.9:g.45401039C>A , CM000677.1:g.45401039C>A | GRCh37 |
| NC_000015.8:g.43188331C>A | NCBI36 |
| NG_009447.1:g.10321G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389039.11:c.1346G>T MANE Select | ENSP00000373691.7:p.Gly449Val | |
| ENST00000389039.10:c.1346G>T | ENSP00000373691.6:p.Gly449Val | |
| ENST00000558383.1:n.2511G>T | ||
| ENST00000603300.1:c.1346G>T | ENSP00000475084.1:p.Gly449Val | |
| NM_014080.4:c.1346G>T | NP_054799.4:p.Gly449Val | |
| XM_005254421.2:c.1346G>T | XP_005254478.1:p.Gly449Val | |
| NM_001363711.1:c.1346G>T | NP_001350640.1:p.Gly449Val | |
| NM_001363711.2:c.1346G>T MANE Select | NP_001350640.1:p.Gly449Val | |
| NM_014080.5:c.1346G>T | NP_054799.4:p.Gly449Val |