Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44291124G>A , CM000683.2:g.44291124G>A | GRCh38 |
| NC_000021.8:g.45711007G>A , CM000683.1:g.45711007G>A | GRCh37 |
| NC_000021.7:g.44535435G>A | NCBI36 |
| NG_009556.1:g.10245G>A , LRG_18:g.10245G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291582.6:c.909G>A MANE Select | ENSP00000291582.5:p.Arg303= | |
| ENST00000291582.5:c.909G>A | ENSP00000291582.5:p.Arg303= | |
| ENST00000337909.5:n.370G>A | ||
| ENST00000397994.8:n.370G>A | ||
| ENST00000527919.5:n.1639G>A | ||
| ENST00000530812.5:n.2656G>A | ||
| NM_000383.3:c.909G>A | NP_000374.1:p.Arg303= | |
| XM_011529551.1:c.906G>A | XP_011527853.1:p.Arg302= | |
| NM_000383.4:c.909G>A MANE Select | NP_000374.1:p.Arg303= |