Linked Data
MyVariant Identifiers:
chr9:g.133353783A>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133353783A>C , CM000671.2:g.133353783A>C | GRCh38 |
| NC_000009.10:g.135210459A>C | NCBI36 |
| NG_008477.1:g.7724T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371974.8:c.481T>G MANE Select | ENSP00000361042.3:p.Tyr161Asp | |
| ENST00000371974.7:c.481T>G | ENSP00000361042.3:p.Tyr161Asp | |
| ENST00000437995.1:n.427T>G | ||
| ENST00000495952.5:n.471T>G | ||
| ENST00000615505.4:c.154T>G | ENSP00000482067.1:p.Tyr52Asp | |
| NM_001280787.1:c.154T>G | NP_001267716.1:p.Tyr52Asp | |
| NM_003172.3:c.481T>G | NP_003163.1:p.Tyr161Asp | |
| XM_011518942.1:c.154T>G | XP_011517244.1:p.Tyr52Asp | |
| NM_003172.4:c.481T>G MANE Select | NP_003163.1:p.Tyr161Asp |