Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.24259586G>A , CM000676.2:g.24259586G>A | GRCh38 |
| NC_000014.8:g.24728792G>A , CM000676.1:g.24728792G>A | GRCh37 |
| NC_000014.7:g.23798632G>A | NCBI36 |
| NG_007150.1:g.8581C>T | |
| NG_007150.2:g.8581C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000206765.11:c.984+118C>T MANE Select | ENSP00000206765.6:n.984+118C>T | |
| ENST00000206765.10:c.984+118C>T | ENSP00000206765.6:n.984+118C>T | |
| ENST00000544573.5:c.-28-1198C>T | ENSP00000439446.1:n.-28-1198C>T | |
| ENST00000559136.1:c.57+118C>T | ENSP00000453337.1:n.57+118C>T | |
| NM_000359.2:c.984+118C>T | NP_000350.1:n.984+118C>T | |
| NM_000359.3:c.984+118C>T MANE Select | NP_000350.1:n.984+118C>T |