Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.38688742A>G , CM000675.2:g.38688742A>G | GRCh38 |
| NC_000013.10:g.39262879A>G , CM000675.1:g.39262879A>G | GRCh37 |
| NC_000013.9:g.38160879A>G | NCBI36 |
| NG_008125.2:g.6707A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_207361.6:c.1398A>G MANE Select | NP_997244.4:p.Gln466= |
| ENST00000280481.9:c.1398A>G MANE Select | ENSP00000280481.7:p.Gln466= |
| NM_207361.5:c.1398A>G | NP_997244.4:p.Gln466= |
| ENST00000280481.8:c.1398A>G | ENSP00000280481.7:p.Gln466= |
| XM_011535057.1:c.1398A>G | XP_011533359.1:p.Gln466= |
| XM_017020554.1:c.1398A>G | XP_016876043.1:p.Gln466= |
| XR_941571.1:n.1706A>G | |
| XR_941571.2:n.1702A>G |