Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31383782G>C , CM000664.2:g.31383782G>C | GRCh38 |
| NC_000002.11:g.31606648G>C , CM000664.1:g.31606648G>C | GRCh37 |
| NC_000002.10:g.31460152G>C | NCBI36 |
| NG_008871.1:g.35964C>G | |
| NG_008871.2:g.35964C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000379.4:c.859C>G MANE Select | NP_000370.2:p.Leu287Val |
| ENST00000379416.4:c.859C>G MANE Select | ENSP00000368727.3:p.Leu287Val |
| NM_000379.3:c.859C>G | NP_000370.2:p.Leu287Val |
| ENST00000379416.3:c.859C>G | ENSP00000368727.3:p.Leu287Val |
| ENST00000476043.1:n.377C>G | |
| ENST00000491727.5:n.402C>G | |
| XM_011533095.1:c.859C>G | XP_011531397.1:p.Leu287Val |
| XM_011533095.2:c.859C>G | XP_011531397.1:p.Leu287Val |
| XM_011533096.1:c.859C>G | XP_011531398.1:p.Leu287Val |
| XM_011533096.2:c.859C>G | XP_011531398.1:p.Leu287Val |