Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94007710C>T , CM000663.2:g.94007710C>T | GRCh38 |
| NC_000001.10:g.94473266C>T , CM000663.1:g.94473266C>T | GRCh37 |
| NC_000001.9:g.94245854C>T | NCBI36 |
| NG_009073.1:g.118440G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.5929G>A MANE Select | ENSP00000359245.3:p.Gly1977Ser | |
| ENST00000370225.3:c.5929G>A | ENSP00000359245.3:p.Gly1977Ser | |
| ENST00000465352.1:n.345G>A | ||
| ENST00000484388.1:n.43G>A | ||
| ENST00000536513.5:c.2305G>A | ENSP00000439707.2:p.Gly769Ser | |
| NM_000350.2:c.5929G>A | NP_000341.2:p.Gly1977Ser | |
| NM_000350.3:c.5929G>A MANE Select | NP_000341.2:p.Gly1977Ser |