Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.93998093A>C , CM000663.2:g.93998093A>C | GRCh38 |
| NC_000001.10:g.94463649A>C , CM000663.1:g.94463649A>C | GRCh37 |
| NC_000001.9:g.94236237A>C | NCBI36 |
| NG_009073.1:g.128057T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.6497T>G MANE Select | ENSP00000359245.3:p.Ile2166Ser | |
| ENST00000370225.3:c.6497T>G | ENSP00000359245.3:p.Ile2166Ser | |
| ENST00000536513.5:c.2873T>G | ENSP00000439707.2:p.Ile958Ser | |
| NM_000350.2:c.6497T>G | NP_000341.2:p.Ile2166Ser | |
| NM_000350.3:c.6497T>G MANE Select | NP_000341.2:p.Ile2166Ser |