Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67586522T>A , CM000673.2:g.67586522T>A | GRCh38 |
| NC_000011.9:g.67353993T>A , CM000673.1:g.67353993T>A | GRCh37 |
| NC_000011.8:g.67110569T>A | NCBI36 |
| NG_012075.1:g.7928T>A , LRG_723:g.7928T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398603.6:c.470T>A | ENSP00000381604.1:p.Phe157Tyr | |
| ENST00000398606.10:c.578T>A MANE Select | ENSP00000381607.3:p.Phe193Tyr | |
| ENST00000398603.5:c.470T>A | ENSP00000381604.1:p.Phe157Tyr | |
| ENST00000398606.7:c.578T>A | ENSP00000381607.3:p.Phe193Tyr | |
| ENST00000467591.1:n.689T>A | ||
| ENST00000494593.1:n.1550T>A | ||
| ENST00000498765.5:c.641T>A | ||
| NM_000852.3:c.578T>A , LRG_723t1:c.578T>A | NP_000843.1:p.Phe193Tyr | |
| NM_000852.4:c.578T>A MANE Select | NP_000843.1:p.Phe193Tyr |