Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.232486499A>G , CM000664.2:g.232486499A>G | GRCh38 |
| NC_000002.11:g.233351209A>G , CM000664.1:g.233351209A>G | GRCh37 |
| NC_000002.10:g.233059453A>G | NCBI36 |
| NG_034065.1:g.6361T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004826.4:c.155T>C MANE Select | NP_004817.2:p.Leu52Pro |
| ENST00000304546.6:c.155T>C MANE Select | ENSP00000302051.1:p.Leu52Pro |
| NM_001290787.1:c.155T>C | NP_001277716.1:p.Leu52Pro |
| NM_001290787.2:c.155T>C | NP_001277716.1:p.Leu52Pro |
| NM_004826.3:c.155T>C | NP_004817.2:p.Leu52Pro |
| ENST00000304546.5:c.155T>C | ENSP00000302051.1:p.Leu52Pro |
| ENST00000409941.1:c.155T>C | ENSP00000386333.1:p.Leu52Pro |
| ENST00000482346.1:n.359T>C |