Linked Data
ClinVar Variation Id:
195152
dbSNP Id:
rs192476178
ExAC:
21:47531412 G / A
gnomAD v2:
21-47531412-G-A
gnomAD v3:
21-46111498-G-A
gnomAD v4:
21-46111498-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.46111498G>A , CM000683.2:g.46111498G>A | GRCh38 |
| NC_000021.8:g.47531412G>A , CM000683.1:g.47531412G>A | GRCh37 |
| NC_000021.7:g.46355840G>A | NCBI36 |
| NG_008675.1:g.18380G>A , LRG_476:g.18380G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397763.6:c.22G>A MANE Plus Clinical | ENSP00000380870.1:p.Val8Met | |
| ENST00000300527.9:c.22G>A MANE Select | ENSP00000300527.4:p.Val8Met | |
| ENST00000409416.6:c.22G>A | ENSP00000387115.1:p.Val8Met | |
| ENST00000300527.8:c.22G>A | ENSP00000300527.4:p.Val8Met | |
| ENST00000310645.9:c.22G>A | ENSP00000312529.5:p.Val8Met | |
| ENST00000397763.5:c.22G>A | ENSP00000380870.1:p.Val8Met | |
| ENST00000409416.5:c.22G>A | ENSP00000387115.1:p.Val8Met | |
| ENST00000436769.5:c.22G>A | ENSP00000390418.1:p.Val8Met | |
| NM_001849.3:c.22G>A , LRG_476t1:c.22G>A | NP_001840.3:p.Val8Met | |
| NM_058174.2:c.22G>A | NP_478054.2:p.Val8Met | |
| NM_058175.2:c.22G>A | NP_478055.2:p.Val8Met | |
| XM_011529451.1:c.22G>A | XP_011527753.1:p.Val8Met | |
| XM_011529452.1:c.22G>A | XP_011527754.1:p.Val8Met | |
| XR_937438.1:n.145G>A | ||
| XR_937439.1:n.145G>A | ||
| XR_937438.2:n.152G>A | ||
| XR_937439.2:n.152G>A | ||
| NM_001849.4:c.22G>A MANE Select | NP_001840.3:p.Val8Met | |
| NM_058174.3:c.22G>A MANE Plus Clinical | NP_478054.2:p.Val8Met | |
| NM_058175.3:c.22G>A | NP_478055.2:p.Val8Met |