Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128258178C>T , CM000667.2:g.128258178C>T | GRCh38 |
| NC_000005.9:g.127593870C>T , CM000667.1:g.127593870C>T | GRCh37 |
| NC_000005.8:g.127621769C>T | NCBI36 |
| NG_008750.1:g.284866G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262464.9:c.*1277G>A MANE Select | ENSP00000262464.4:n.*1277G>A | |
| ENST00000262464.8:c.*1277G>A | ENSP00000262464.4:n.*1277G>A | |
| ENST00000508053.5:c.*1277G>A | ENSP00000424571.1:n.*1277G>A | |
| ENST00000619499.4:c.10013G>A | ENSP00000482132.1:n.10013G>A | |
| NM_001999.3:c.*1277G>A | NP_001990.2:n.*1277G>A | |
| NM_001999.4:c.*1277G>A MANE Select | NP_001990.2:n.*1277G>A |