Linked Data
MyVariant Identifiers:
chr10:g.96748662C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94988905C>G , CM000672.2:g.94988905C>G | GRCh38 |
| NC_000010.10:g.96748662C>G , CM000672.1:g.96748662C>G | GRCh37 |
| NC_000010.9:g.96738652C>G | NCBI36 |
| NG_008385.1:g.55248C>G | |
| NG_008385.2:g.55748C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.1350C>G MANE Select | ENSP00000260682.6:p.Thr450= | |
| ENST00000643112.1:c.*359C>G | ENSP00000496202.1:n.*359C>G | |
| ENST00000260682.6:c.1350C>G | ENSP00000260682.6:p.Thr450= | |
| NM_000771.3:c.1350C>G | NP_000762.2:p.Thr450= | |
| NM_000771.4:c.1350C>G MANE Select | NP_000762.2:p.Thr450= |