Linked Data
MyVariant Identifiers:
chr15:g.75042517C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74750176C>G , CM000677.2:g.74750176C>G | GRCh38 |
| NC_000015.9:g.75042517C>G , CM000677.1:g.75042517C>G | GRCh37 |
| NC_000015.8:g.72829570C>G | NCBI36 |
| NG_008431.1:g.32635C>G | |
| NG_008431.2:g.32635C>G | |
| NG_061543.1:g.6332C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343932.5:c.438C>G MANE Select | ENSP00000342007.4:p.Thr146= | |
| ENST00000343932.4:c.438C>G | ENSP00000342007.4:p.Thr146= | |
| NM_000761.4:c.438C>G | NP_000752.2:p.Thr146= | |
| NM_000761.5:c.438C>G MANE Select | NP_000752.2:p.Thr146= |