Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31269128G>T , CM000668.2:g.31269128G>T | GRCh38 |
| NC_000006.11:g.31236905G>T , CM000668.1:g.31236905G>T | GRCh37 |
| NC_000006.10:g.31344884G>T | NCBI36 |
| NG_029422.2:g.8004C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.*41C>A MANE Select | ENSP00000365402.5:n.*41C>A | |
| ENST00000376228.9:c.*41C>A | ENSP00000365402.5:n.*41C>A | |
| ENST00000376237.8:c.*729C>A | ENSP00000365412.4:n.*729C>A | |
| ENST00000383329.7:c.*41C>A | ENSP00000372819.3:n.*41C>A | |
| ENST00000466892.5:n.375C>A | ||
| ENST00000470363.5:n.900C>A | ||
| ENST00000487245.5:n.1501C>A | ||
| NM_002117.5:c.*41C>A | NP_002108.4:n.*41C>A | |
| NM_002117.6:c.*41C>A MANE Select | NP_002108.4:n.*41C>A |