Linked Data
MyVariant Identifiers:
chr10:g.17849684C>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.17849684C>G , CM000672.2:g.17849684C>G | GRCh38 |
| NG_047011.1:g.45342C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000569591.3:c.1169C>G MANE Select | ENSP00000455897.1:p.Thr390Ser | |
| ENST00000569591.2:c.1169C>G | ENSP00000455897.1:p.Thr390Ser | |
| NM_002438.3:c.1169C>G | NP_002429.1:p.Thr390Ser | |
| NM_002438.4:c.1169C>G MANE Select | NP_002429.1:p.Thr390Ser |