Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160882129C>G , CM000663.2:g.160882129C>G | GRCh38 |
| NC_000001.10:g.160851919C>G , CM000663.1:g.160851919C>G | GRCh37 |
| NC_000001.9:g.159118543C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326245.4:c.233G>C MANE Select | ENSP00000323587.3:p.Gly78Ala | |
| ENST00000326245.3:c.233G>C | ENSP00000323587.3:p.Gly78Ala | |
| ENST00000464077.1:n.167G>C | ||
| NM_017625.2:c.233G>C | NP_060095.2:p.Gly78Ala | |
| NM_017625.3:c.233G>C MANE Select | NP_060095.2:p.Gly78Ala |