Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.12069034A>G , CM000672.2:g.12069034A>G | GRCh38 |
| NC_000010.10:g.12111033A>G , CM000672.1:g.12111033A>G | GRCh37 |
| NC_000010.9:g.12151039A>G | NCBI36 |
| NG_033248.1:g.5118A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_018706.7:c.1A>G MANE Select | NP_061176.4:p.Met1Val |
| ENST00000263035.9:c.1A>G MANE Select | ENSP00000263035.4:p.Met1Val |
| NM_018706.6:c.1A>G | NP_061176.3:p.Met1Val |
| ENST00000263035.8:c.1A>G | ENSP00000263035.4:p.Met1Val |
| ENST00000437298.1:c.1A>G | ENSP00000388163.1:p.Met1Val |