Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.35383119T>A , CM000684.2:g.35383119T>A | GRCh38 |
| NC_000022.10:g.35779112T>A , CM000684.1:g.35779112T>A | GRCh37 |
| NC_000022.9:g.34109112T>A | NCBI36 |
| NG_023030.1:g.7053T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216117.9:c.37T>A MANE Select | ENSP00000216117.8:p.Leu13Met | |
| ENST00000481190.2:c.170T>A | ENSP00000503987.1:p.Phe57Tyr | |
| ENST00000677931.1:c.37T>A | ENSP00000502849.1:p.Leu13Met | |
| ENST00000679074.1:c.37T>A | ENSP00000503459.1:p.Leu13Met | |
| ENST00000216117.8:c.37T>A | ENSP00000216117.8:p.Leu13Met | |
| ENST00000412893.5:c.37T>A | ENSP00000413316.1:p.Leu13Met | |
| ENST00000481190.1:n.251T>A | ||
| NM_002133.2:c.37T>A | NP_002124.1:p.Leu13Met | |
| NM_002133.3:c.37T>A MANE Select | NP_002124.1:p.Leu13Met |