Linked Data
dbSNP Id:
rs754020959
ExAC:
10:75830825 A / G
gnomAD v2:
10-75830825-A-G
gnomAD v4:
10-74071067-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.74071067A>G , CM000672.2:g.74071067A>G | GRCh38 |
| NC_000010.10:g.75830825A>G , CM000672.1:g.75830825A>G | GRCh37 |
| NC_000010.9:g.75500831A>G | NCBI36 |
| NG_008868.1:g.77954A>G , LRG_383:g.77954A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000211998.10:c.483A>G MANE Select | ENSP00000211998.5:p.Thr161= | |
| ENST00000211998.8:c.483A>G | ENSP00000211998.4:p.Thr161= | |
| ENST00000372755.7:c.483A>G | ENSP00000361841.3:p.Thr161= | |
| ENST00000478896.2:n.331+27914A>G | ||
| ENST00000623461.3:n.441A>G | ||
| ENST00000624354.3:c.*238A>G | ENSP00000485551.1:n.*238A>G | |
| NM_003373.3:c.483A>G | NP_003364.1:p.Thr161= | |
| NM_014000.2:c.483A>G , LRG_383t1:c.483A>G | NP_054706.1:p.Thr161= | |
| XM_005270142.1:c.483A>G | XP_005270199.1:p.Thr161= | |
| XM_005270143.1:c.483A>G | XP_005270200.1:p.Thr161= | |
| NM_003373.4:c.483A>G | NP_003364.1:p.Thr161= | |
| NM_014000.3:c.483A>G MANE Select | NP_054706.1:p.Thr161= |