Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.108084675T>C , CM000685.2:g.108084675T>C | GRCh38 |
| NC_000023.10:g.107327905T>C , CM000685.1:g.107327905T>C | GRCh37 |
| NC_000023.9:g.107214561T>C | NCBI36 |
| NG_012521.1:g.11944A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000217958.8:c.*299A>G MANE Select | ENSP00000217958.3:n.*299A>G | |
| ENST00000217958.7:c.*299A>G | ENSP00000217958.3:n.*299A>G | |
| ENST00000372296.5:c.*445A>G | ENSP00000361370.1:n.*445A>G | |
| NM_002814.3:c.*299A>G | NP_002805.1:n.*299A>G | |
| NM_170750.2:c.*445A>G | NP_736606.1:n.*445A>G | |
| NM_002814.4:c.*299A>G MANE Select | NP_002805.1:n.*299A>G | |
| NM_170750.3:c.*445A>G | NP_736606.1:n.*445A>G |