Linked Data
MyVariant Identifiers:
chr9:g.133353798T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133353798T>C , CM000671.2:g.133353798T>C | GRCh38 |
| NC_000009.10:g.135210474T>C | NCBI36 |
| NG_008477.1:g.7709A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371974.8:c.466A>G MANE Select | ENSP00000361042.3:p.Thr156Ala | |
| ENST00000371974.7:c.466A>G | ENSP00000361042.3:p.Thr156Ala | |
| ENST00000437995.1:n.412A>G | ||
| ENST00000495952.5:n.456A>G | ||
| ENST00000615505.4:c.139A>G | ENSP00000482067.1:p.Thr47Ala | |
| NM_001280787.1:c.139A>G | NP_001267716.1:p.Thr47Ala | |
| NM_003172.3:c.466A>G | NP_003163.1:p.Thr156Ala | |
| XM_011518942.1:c.139A>G | XP_011517244.1:p.Thr47Ala | |
| NM_003172.4:c.466A>G MANE Select | NP_003163.1:p.Thr156Ala |