Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52028024A>G , CM000666.2:g.52028024A>G | GRCh38 |
| NC_000004.11:g.52894190A>G , CM000666.1:g.52894190A>G | GRCh37 |
| NC_000004.10:g.52588947A>G | NCBI36 |
| NG_008891.1:g.15296T>C , LRG_204:g.15296T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000381431.10:c.697T>C MANE Select | ENSP00000370839.6:p.Phe233Leu | |
| ENST00000381431.9:c.697T>C | ENSP00000370839.5:p.Phe233Leu | |
| NM_000232.4:c.697T>C , LRG_204t1:c.697T>C | NP_000223.1:p.Phe233Leu | |
| XM_006714049.2:c.400T>C | XP_006714112.1:p.Phe134Leu | |
| XM_011534403.1:c.487T>C | XP_011532705.1:p.Phe163Leu | |
| XM_011534404.1:c.400T>C | XP_011532706.1:p.Phe134Leu | |
| NM_000232.5:c.697T>C MANE Select | NP_000223.1:p.Phe233Leu |