Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94060544A>T , CM000663.2:g.94060544A>T | GRCh38 |
| NC_000001.10:g.94526100A>T , CM000663.1:g.94526100A>T | GRCh37 |
| NC_000001.9:g.94298688A>T | NCBI36 |
| NG_009073.1:g.65606T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.2153T>A MANE Select | ENSP00000359245.3:p.Phe718Tyr | |
| ENST00000649773.1:c.2153T>A | ENSP00000496882.1:p.Phe718Tyr | |
| ENST00000370225.3:c.2153T>A | ENSP00000359245.3:p.Phe718Tyr | |
| ENST00000472033.1:n.273T>A | ||
| ENST00000536513.5:c.-65+2630T>A | ENSP00000439707.2:n.-65+2630T>A | |
| NM_000350.2:c.2153T>A | NP_000341.2:p.Phe718Tyr | |
| NM_000350.3:c.2153T>A MANE Select | NP_000341.2:p.Phe718Tyr |