Linked Data
gnomAD v4:
21-44290053-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44290053C>G , CM000683.2:g.44290053C>G | GRCh38 |
| NC_000021.8:g.45709936C>G , CM000683.1:g.45709936C>G | GRCh37 |
| NC_000021.7:g.44534364C>G | NCBI36 |
| NG_009556.1:g.9174C>G , LRG_18:g.9174C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291582.6:c.864C>G MANE Select | ENSP00000291582.5:p.Asp288Glu | |
| ENST00000291582.5:c.864C>G | ENSP00000291582.5:p.Asp288Glu | |
| ENST00000527919.5:n.1597C>G | ||
| ENST00000530812.5:n.2614C>G | ||
| NM_000383.3:c.864C>G | NP_000374.1:p.Asp288Glu | |
| XM_011529551.1:c.864C>G | XP_011527853.1:p.Asp288Glu | |
| NM_000383.4:c.864C>G MANE Select | NP_000374.1:p.Asp288Glu |