Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.14978113T>A , CM000674.2:g.14978113T>A | GRCh38 |
| NC_000012.11:g.15131047T>A , CM000674.1:g.15131047T>A | GRCh37 |
| NC_000012.10:g.15022314T>A | NCBI36 |
| NG_016859.1:g.10092T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266395.3:c.101T>A MANE Select | ENSP00000266395.2:p.Phe34Tyr | |
| ENST00000266395.2:c.101T>A | ENSP00000266395.2:p.Phe34Tyr | |
| NM_006205.2:c.101T>A | NP_006196.1:p.Phe34Tyr | |
| XR_931376.1:n.175+11374A>T | ||
| XM_017019431.2:c.101T>A | XP_016874920.1:p.Phe34Tyr | |
| XR_931376.2:n.389+11374A>T | ||
| NM_006205.3:c.101T>A MANE Select | NP_006196.1:p.Phe34Tyr |