Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31334620C>A , CM000664.2:g.31334620C>A | GRCh38 |
| NC_000002.11:g.31557486C>A , CM000664.1:g.31557486C>A | GRCh37 |
| NC_000002.10:g.31410990C>A | NCBI36 |
| NG_008871.1:g.85126G>T | |
| NG_008871.2:g.85126G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379416.4:c.*1338G>T MANE Select | ENSP00000368727.3:n.*1338G>T | |
| ENST00000379416.3:c.*1338G>T | ENSP00000368727.3:n.*1338G>T | |
| NM_000379.3:c.*1338G>T | NP_000370.2:n.*1338G>T | |
| XM_011533095.1:c.*1338G>T | XP_011531397.1:n.*1338G>T | |
| XM_011533095.2:c.*1338G>T | XP_011531397.1:n.*1338G>T | |
| NM_000379.4:c.*1338G>T MANE Select | NP_000370.2:n.*1338G>T |