Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102527825C>A , CM000673.2:g.102527825C>A | GRCh38 |
| NC_000011.9:g.102398556C>A , CM000673.1:g.102398556C>A | GRCh37 |
| NC_000011.8:g.101903766C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260227.5:c.267G>T MANE Select | ENSP00000260227.4:p.Val89= | |
| ENST00000260227.4:c.267G>T | ENSP00000260227.4:p.Val89= | |
| ENST00000531200.1:n.314G>T | ||
| ENST00000533366.5:n.317G>T | ||
| NM_002423.3:c.267G>T | NP_002414.1:p.Val89= | |
| NM_002423.4:c.267G>T | NP_002414.1:p.Val89= | |
| NM_002423.5:c.267G>T MANE Select | NP_002414.1:p.Val89= |