Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128305064T>A , CM000667.2:g.128305064T>A | GRCh38 |
| NC_000005.9:g.127640756T>A , CM000667.1:g.127640756T>A | GRCh37 |
| NC_000005.8:g.127668655T>A | NCBI36 |
| NG_008750.1:g.237980A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703783.1:n.2477A>T | ||
| ENST00000703785.1:n.2396A>T | ||
| ENST00000262464.9:c.5693A>T MANE Select | ENSP00000262464.4:p.Glu1898Val | |
| ENST00000262464.8:c.5693A>T | ENSP00000262464.4:p.Glu1898Val | |
| ENST00000508053.5:c.5693A>T | ENSP00000424571.1:p.Glu1898Val | |
| ENST00000619499.4:c.5690A>T | ENSP00000482132.1:p.Glu1897Val | |
| NM_001999.3:c.5693A>T | NP_001990.2:p.Glu1898Val | |
| XM_017009228.2:c.5540A>T | XP_016864717.1:p.Glu1847Val | |
| NM_001999.4:c.5693A>T MANE Select | NP_001990.2:p.Glu1898Val |