Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218812658A>G , CM000664.2:g.218812658A>G | GRCh38 |
| NC_000002.11:g.219677381A>G , CM000664.1:g.219677381A>G | GRCh37 |
| NC_000002.10:g.219385625A>G | NCBI36 |
| NG_007959.1:g.35910A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258415.9:c.753A>G MANE Select | ENSP00000258415.4:p.Ser251= | |
| ENST00000258415.8:c.753A>G | ENSP00000258415.4:p.Ser251= | |
| ENST00000411688.1:c.471A>G | ENSP00000392671.1:p.Ser157= | |
| ENST00000445971.1:c.*214A>G | ENSP00000404945.1:n.*214A>G | |
| ENST00000466602.1:n.701A>G | ||
| ENST00000494263.5:n.1187A>G | ||
| NM_000784.3:c.753A>G | NP_000775.1:p.Ser251= | |
| XM_017003488.2:c.333A>G | XP_016858977.1:p.Ser111= | |
| NM_000784.4:c.753A>G MANE Select | NP_000775.1:p.Ser251= |