Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44289826G>A , CM000683.2:g.44289826G>A | GRCh38 |
| NC_000021.8:g.45709709G>A , CM000683.1:g.45709709G>A | GRCh37 |
| NC_000021.7:g.44534137G>A | NCBI36 |
| NG_009556.1:g.8947G>A , LRG_18:g.8947G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291582.6:c.798+24G>A MANE Select | ENSP00000291582.5:n.798+24G>A | |
| ENST00000291582.5:c.798+24G>A | ENSP00000291582.5:n.798+24G>A | |
| ENST00000527919.5:n.1531+24G>A | ||
| ENST00000530812.5:n.2548+24G>A | ||
| NM_000383.3:c.798+24G>A | NP_000374.1:n.798+24G>A | |
| XM_011529551.1:c.798+24G>A | XP_011527853.1:n.798+24G>A | |
| NM_000383.4:c.798+24G>A MANE Select | NP_000374.1:n.798+24G>A |