Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57764093C>T , CM000674.2:g.57764093C>T | GRCh38 |
| NC_000012.11:g.58157876C>T , CM000674.1:g.58157876C>T | GRCh37 |
| NC_000012.10:g.56444143C>T | NCBI36 |
| NG_007076.1:g.8101G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000713544.1:c.1296+5G>A | ENSP00000518840.1:n.1296+5G>A | |
| ENST00000713545.1:c.*220+5G>A | ENSP00000518841.1:n.*220+5G>A | |
| ENST00000228606.9:c.1215+5G>A MANE Select | ENSP00000228606.4:n.1215+5G>A | |
| ENST00000228606.8:c.1215+5G>A | ENSP00000228606.4:n.1215+5G>A | |
| ENST00000547344.5:n.1354+5G>A | ||
| NM_000785.3:c.1215+5G>A | NP_000776.1:n.1215+5G>A | |
| NM_000785.4:c.1215+5G>A MANE Select | NP_000776.1:n.1215+5G>A |