Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.42688162G>T , CM000665.2:g.42688162G>T | GRCh38 |
| NC_000003.11:g.42729654G>T , CM000665.1:g.42729654G>T | GRCh37 |
| NC_000003.10:g.42704658G>T | NCBI36 |
| NG_033035.1:g.7644G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000287777.5:c.1173G>T MANE Select | ENSP00000287777.4:p.Glu391Asp | |
| ENST00000287777.4:c.1173G>T | ENSP00000287777.4:p.Glu391Asp | |
| NM_152393.3:c.1173G>T | NP_689606.2:p.Glu391Asp | |
| XM_005264866.2:c.1173G>T | XP_005264923.1:p.Glu391Asp | |
| NM_152393.4:c.1173G>T MANE Select | NP_689606.2:p.Glu391Asp |