Linked Data
MyVariant Identifiers:
chr21:g.43172110T>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.43172110T>G , CM000683.2:g.43172110T>G | GRCh38 |
| NG_009823.1:g.8080T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291554.6:c.352T>G MANE Select | ENSP00000291554.2:p.Tyr118Asp | |
| ENST00000398132.1:c.241T>G | ENSP00000381200.1:p.Tyr81Asp | |
| ENST00000398133.5:c.292T>G | ENSP00000381201.1:p.Tyr98Asp | |
| ENST00000468016.1:n.453T>G | ||
| ENST00000482775.1:n.433T>G | ||
| NM_000394.3:c.352T>G | NP_000385.1:p.Tyr118Asp | |
| XM_005261093.2:c.241T>G | XP_005261150.1:p.Tyr81Asp | |
| NM_001363766.1:c.241T>G | NP_001350695.1:p.Tyr81Asp | |
| NM_000394.4:c.352T>G MANE Select | NP_000385.1:p.Tyr118Asp |