Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1416101T>A , CM000667.2:g.1416101T>A | GRCh38 |
| NC_000005.9:g.1416216T>A , CM000667.1:g.1416216T>A | GRCh37 |
| NC_000005.8:g.1469216T>A | NCBI36 |
| NG_015885.1:g.34328A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000270349.12:c.1028A>T MANE Select | ENSP00000270349.9:p.Tyr343Phe | |
| ENST00000270349.11:c.1028A>T | ENSP00000270349.9:p.Tyr343Phe | |
| ENST00000511750.1:n.478A>T | ||
| NM_001044.4:c.1028A>T | NP_001035.1:p.Tyr343Phe | |
| NM_001044.5:c.1028A>T MANE Select | NP_001035.1:p.Tyr343Phe |