Linked Data
MyVariant Identifiers:
chr14:g.37132691C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.36663486C>T , CM000676.2:g.36663486C>T | GRCh38 |
| NC_000014.8:g.37132691C>T , CM000676.1:g.37132691C>T | GRCh37 |
| NC_000014.7:g.36202442C>T | NCBI36 |
| NG_013357.1:g.10919C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361487.7:c.594C>T MANE Select | ENSP00000355245.6:p.Val198= | |
| ENST00000361487.6:c.594C>T | ENSP00000355245.6:p.Val198= | |
| ENST00000402703.6:c.594C>T | ENSP00000384817.2:p.Val198= | |
| ENST00000554201.1:c.33C>T | ENSP00000450434.1:p.Val11= | |
| NM_006194.3:c.594C>T | NP_006185.1:p.Val198= | |
| NM_001372076.1:c.594C>T MANE Select | NP_001359005.1:p.Val198= | |
| NM_006194.4:c.594C>T | NP_006185.1:p.Val198= |