Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17022716C>A , CM000663.2:g.17022716C>A | GRCh38 |
| NC_000001.10:g.17349211C>A , CM000663.1:g.17349211C>A | GRCh37 |
| NC_000001.9:g.17221798C>A | NCBI36 |
| NG_012340.1:g.36455G>T , LRG_316:g.36455G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463045.3:c.486G>T | ENSP00000481376.2:p.Met162Ile | |
| ENST00000491274.6:c.615G>T | ENSP00000480482.2:p.Met205Ile | |
| ENST00000375499.8:c.657G>T MANE Select | ENSP00000364649.3:p.Met219Ile | |
| ENST00000375499.7:c.657G>T | ENSP00000364649.3:p.Met219Ile | |
| ENST00000475049.5:n.82G>T | ||
| ENST00000485092.5:n.321G>T | ||
| ENST00000485515.5:n.591G>T | ||
| NM_003000.2:c.657G>T , LRG_316t1:c.657G>T | NP_002991.2:p.Met219Ile | |
| NM_003000.3:c.657G>T MANE Select | NP_002991.2:p.Met219Ile |