Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.43169497G>A , CM000683.2:g.43169497G>A | GRCh38 |
| NG_009823.1:g.5467G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291554.6:c.189+209G>A MANE Select | ENSP00000291554.2:n.189+209G>A | |
| ENST00000482775.1:n.203-36G>A | ||
| NM_000394.3:c.189+209G>A | NP_000385.1:n.189+209G>A | |
| XR_001755073.1:n.647+1540C>T | ||
| NM_000394.4:c.189+209G>A MANE Select | NP_000385.1:n.189+209G>A |