Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44294400G>A , CM000683.2:g.44294400G>A | GRCh38 |
| NC_000021.8:g.45714283G>A , CM000683.1:g.45714283G>A | GRCh37 |
| NC_000021.7:g.44538711G>A | NCBI36 |
| NG_009556.1:g.13521G>A , LRG_18:g.13521G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000383.4:c.1401-1G>A MANE Select | NP_000374.1:n.1401-1G>A |
| ENST00000291582.6:c.1401-1G>A MANE Select | ENSP00000291582.5:n.1401-1G>A |
| NM_000383.3:c.1401-1G>A | NP_000374.1:n.1401-1G>A |
| ENST00000291582.5:c.1401-1G>A | ENSP00000291582.5:n.1401-1G>A |
| ENST00000337909.5:n.862-1G>A | |
| ENST00000397994.8:n.780-1G>A | |
| ENST00000527919.5:n.2159G>A | |
| ENST00000530812.5:n.3148-1G>A | |
| XM_011529551.1:c.1398-1G>A | XP_011527853.1:n.1398-1G>A |