Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118168654G>T , CM000673.2:g.118168654G>T | GRCh38 |
| NC_000011.9:g.118039369G>T , CM000673.1:g.118039369G>T | GRCh37 |
| NC_000011.8:g.117544579G>T | NCBI36 |
| NG_042217.1:g.12969C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000278947.6:c.168C>A MANE Select | ENSP00000278947.5:p.Tyr56Ter | |
| ENST00000658882.1:c.272C>A | ENSP00000499572.1:p.Thr91Lys | |
| ENST00000665446.1:n.404C>A | ||
| ENST00000669850.1:n.410C>A | ||
| ENST00000278947.5:c.168C>A | ENSP00000278947.5:p.Tyr56Ter | |
| NM_004588.4:c.168C>A | NP_004579.1:p.Tyr56Ter | |
| NM_004588.5:c.168C>A MANE Select | NP_004579.1:p.Tyr56Ter |