Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.136676607A>T , CM000671.2:g.136676607A>T | GRCh38 |
| NC_000009.11:g.139571059A>T , CM000671.1:g.139571059A>T | GRCh37 |
| NC_000009.10:g.138690880A>T | NCBI36 |
| NG_008090.1:g.15853T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371696.7:c.566T>A MANE Select | ENSP00000360761.2:p.Phe189Tyr | |
| ENST00000371694.7:c.492+354T>A | ENSP00000360759.3:n.492+354T>A | |
| ENST00000371696.6:c.566T>A | ENSP00000360761.2:p.Phe189Tyr | |
| ENST00000472820.1:n.494T>A | ||
| ENST00000538402.1:c.566T>A | ENSP00000438919.1:p.Phe189Tyr | |
| NM_001012727.1:c.492+354T>A | NP_001012745.1:n.492+354T>A | |
| NM_006412.3:c.566T>A | NP_006403.2:p.Phe189Tyr | |
| NM_006412.4:c.566T>A MANE Select | NP_006403.2:p.Phe189Tyr | |
| NM_001012727.2:c.492+354T>A | NP_001012745.1:n.492+354T>A |