Linked Data
ClinVar Variation Id:
821127
dbSNP Id:
rs1588876509
MyVariant Identifiers:
chr10:g.43613879G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.43118431G>A , CM000672.2:g.43118431G>A | GRCh38 |
| NC_000010.10:g.43613879G>A , CM000672.1:g.43613879G>A | GRCh37 |
| NC_000010.9:g.42933885G>A | NCBI36 |
| NG_007489.1:g.46363G>A , LRG_518:g.46363G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000615310.5:c.1947G>A | ENSP00000480088.2:p.Gln649= | |
| ENST00000683007.1:n.1917G>A | ||
| ENST00000683872.1:n.1908G>A | ||
| ENST00000340058.6:c.2343G>A | ENSP00000344798.4:p.Gln781= | |
| ENST00000355710.8:c.2343G>A MANE Select | ENSP00000347942.3:p.Gln781= | |
| ENST00000671844.1:c.*937G>A | ENSP00000500541.1:n.*937G>A | |
| ENST00000672389.1:c.*937G>A | ENSP00000500252.1:n.*937G>A | |
| ENST00000340058.5:c.2343G>A | ENSP00000344798.4:p.Gln781= | |
| ENST00000355710.7:c.2343G>A | ENSP00000347942.3:p.Gln781= | |
| ENST00000615310.4:c.1290-1271G>A | ENSP00000480088.1:n.1290-1271G>A | |
| NM_020630.4:c.2343G>A , LRG_518t2:c.2343G>A | NP_065681.1:p.Gln781= | |
| NM_020975.4:c.2343G>A , LRG_518t1:c.2343G>A | NP_066124.1:p.Gln781= | |
| XM_011540027.1:c.2343G>A | XP_011538329.1:p.Gln781= | |
| NM_001355216.1:c.1581G>A | NP_001342145.1:p.Gln527= | |
| NM_020630.5:c.2343G>A | NP_065681.1:p.Gln781= | |
| NM_020975.5:c.2343G>A | NP_066124.1:p.Gln781= | |
| NM_020975.6:c.2343G>A MANE Select | NP_066124.1:p.Gln781= | |
| NM_020630.6:c.2343G>A | NP_065681.1:p.Gln781= |