Linked Data
MyVariant Identifiers:
chr14:g.101349287G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.100882950G>T , CM000676.2:g.100882950G>T | GRCh38 |
| NC_000014.8:g.101349287G>T , CM000676.1:g.101349287G>T | GRCh37 |
| NC_000014.7:g.100419040G>T | NCBI36 |
| NG_045001.1:g.6898C>A | |
| NG_045000.5:g.51682G>T | |
| NG_045000.6:g.51682G>T | |
| NG_045001.2:g.25773C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649591.1:c.1839C>A MANE Select | ENSP00000497482.1:p.Thr613= | |
| ENST00000534062.1:c.1839C>A | ENSP00000435342.1:p.Thr613= | |
| NM_001134888.2:c.1839C>A | NP_001128360.1:p.Thr613= | |
| NM_001134888.3:c.1839C>A MANE Select | NP_001128360.1:p.Thr613= |