Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.173232622T>C , CM000667.2:g.173232622T>C | GRCh38 |
| NC_000005.9:g.172659625T>C , CM000667.1:g.172659625T>C | GRCh37 |
| NC_000005.8:g.172592231T>C | NCBI36 |
| NG_013340.1:g.7691A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329198.5:c.922A>G MANE Select | ENSP00000327758.4:p.Ile308Val | |
| ENST00000329198.4:c.922A>G | ENSP00000327758.4:p.Ile308Val | |
| NM_001166175.1:c.*875A>G | NP_001159647.1:n.*875A>G | |
| NM_001166176.1:c.*721A>G | NP_001159648.1:n.*721A>G | |
| NM_004387.3:c.922A>G | NP_004378.1:p.Ile308Val | |
| NM_004387.4:c.922A>G MANE Select | NP_004378.1:p.Ile308Val | |
| NM_001166175.2:c.*875A>G | NP_001159647.1:n.*875A>G | |
| NM_001166176.2:c.*721A>G | NP_001159648.1:n.*721A>G |