Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128305012G>T , CM000667.2:g.128305012G>T | GRCh38 |
| NC_000005.9:g.127640704G>T , CM000667.1:g.127640704G>T | GRCh37 |
| NC_000005.8:g.127668603G>T | NCBI36 |
| NG_008750.1:g.238032C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703783.1:n.2529C>A | ||
| ENST00000703785.1:n.2448C>A | ||
| ENST00000262464.9:c.5745C>A MANE Select | ENSP00000262464.4:p.Tyr1915Ter | |
| ENST00000262464.8:c.5745C>A | ENSP00000262464.4:p.Tyr1915Ter | |
| ENST00000508053.5:c.5745C>A | ENSP00000424571.1:p.Tyr1915Ter | |
| ENST00000619499.4:c.5742C>A | ENSP00000482132.1:p.Tyr1914Ter | |
| NM_001999.3:c.5745C>A | NP_001990.2:p.Tyr1915Ter | |
| XM_017009228.2:c.5592C>A | XP_016864717.1:p.Tyr1864Ter | |
| NM_001999.4:c.5745C>A MANE Select | NP_001990.2:p.Tyr1915Ter |