Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159320335T>A , CM000667.2:g.159320335T>A | GRCh38 |
| NC_000005.9:g.158747343T>A , CM000667.1:g.158747343T>A | GRCh37 |
| NC_000005.8:g.158679921T>A | NCBI36 |
| NG_009618.1:g.15139A>T , LRG_71:g.15139A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696750.1:c.38A>T | ENSP00000512849.1:p.Tyr13Phe | |
| ENST00000696751.1:c.*163A>T | ENSP00000512850.1:n.*163A>T | |
| ENST00000231228.3:c.668A>T MANE Select | ENSP00000231228.2:p.Tyr223Phe | |
| ENST00000231228.2:c.668A>T | ENSP00000231228.2:p.Tyr223Phe | |
| NM_002187.2:c.668A>T , LRG_71t1:c.668A>T | NP_002178.2:p.Tyr223Phe | |
| NM_002187.3:c.668A>T MANE Select | NP_002178.2:p.Tyr223Phe |