Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122461736C>G , CM000672.2:g.122461736C>G | GRCh38 |
| NC_000010.10:g.124221252C>G , CM000672.1:g.124221252C>G | GRCh37 |
| NC_000010.9:g.124211242C>G | NCBI36 |
| NG_011554.1:g.5212C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.84C>G MANE Select | ENSP00000357980.3:p.Gly28= | |
| ENST00000648167.1:c.154+3027C>G | ENSP00000498033.1:n.154+3027C>G | |
| ENST00000368984.7:c.84C>G | ENSP00000357980.3:p.Gly28= | |
| NM_002775.4:c.84C>G | NP_002766.1:p.Gly28= | |
| NM_002775.5:c.84C>G MANE Select | NP_002766.1:p.Gly28= |