Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94007652G>A , CM000663.2:g.94007652G>A | GRCh38 |
| NC_000001.10:g.94473208G>A , CM000663.1:g.94473208G>A | GRCh37 |
| NC_000001.9:g.94245796G>A | NCBI36 |
| NG_009073.1:g.118498C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.5987C>T MANE Select | ENSP00000359245.3:p.Ala1996Val | |
| ENST00000370225.3:c.5987C>T | ENSP00000359245.3:p.Ala1996Val | |
| ENST00000465352.1:n.403C>T | ||
| ENST00000484388.1:n.101C>T | ||
| ENST00000536513.5:c.2363C>T | ENSP00000439707.2:p.Ala788Val | |
| NM_000350.2:c.5987C>T | NP_000341.2:p.Ala1996Val | |
| NM_000350.3:c.5987C>T MANE Select | NP_000341.2:p.Ala1996Val |