Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94008246G>T , CM000663.2:g.94008246G>T | GRCh38 |
| NC_000001.10:g.94473802G>T , CM000663.1:g.94473802G>T | GRCh37 |
| NC_000001.9:g.94246390G>T | NCBI36 |
| NG_009073.1:g.117904C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.5887C>A MANE Select | ENSP00000359245.3:p.Arg1963Ser | |
| ENST00000370225.3:c.5887C>A | ENSP00000359245.3:p.Arg1963Ser | |
| ENST00000465352.1:n.303C>A | ||
| ENST00000536513.5:c.2263C>A | ENSP00000439707.2:p.Arg755Ser | |
| NM_000350.2:c.5887C>A | NP_000341.2:p.Arg1963Ser | |
| NM_000350.3:c.5887C>A MANE Select | NP_000341.2:p.Arg1963Ser |