Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46687198T>G , CM000682.2:g.46687198T>G | GRCh38 |
| NC_000020.10:g.45315837T>G , CM000682.1:g.45315837T>G | GRCh37 |
| NC_000020.9:g.44749244T>G | NCBI36 |
| NG_047182.1:g.2288A>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_033550.4:c.317A>C MANE Select | NP_291028.3:p.Tyr106Ser |
| ENST00000372114.4:c.317A>C MANE Select | ENSP00000361186.3:p.Tyr106Ser |
| NM_033550.3:c.317A>C | NP_291028.3:p.Tyr106Ser |
| ENST00000372102.3:c.322A>C | ENSP00000361174.3:p.Met108Leu |
| ENST00000372114.3:c.317A>C | ENSP00000361186.3:p.Tyr106Ser |