Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52028021T>C , CM000666.2:g.52028021T>C | GRCh38 |
| NC_000004.11:g.52894187T>C , CM000666.1:g.52894187T>C | GRCh37 |
| NC_000004.10:g.52588944T>C | NCBI36 |
| NG_008891.1:g.15299A>G , LRG_204:g.15299A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000381431.10:c.700A>G MANE Select | ENSP00000370839.6:p.Ile234Val | |
| ENST00000381431.9:c.700A>G | ENSP00000370839.5:p.Ile234Val | |
| NM_000232.4:c.700A>G , LRG_204t1:c.700A>G | NP_000223.1:p.Ile234Val | |
| XM_006714049.2:c.403A>G | XP_006714112.1:p.Ile135Val | |
| XM_011534403.1:c.490A>G | XP_011532705.1:p.Ile164Val | |
| XM_011534404.1:c.403A>G | XP_011532706.1:p.Ile135Val | |
| NM_000232.5:c.700A>G MANE Select | NP_000223.1:p.Ile234Val |