Linked Data
ClinVar Variation Id:
45852
dbSNP Id:
rs113317262
ExAC:
17:39925442 C / T
gnomAD v2:
17-39925442-C-T
gnomAD v3:
17-41769190-C-T
gnomAD v4:
17-41769190-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41769190C>T , CM000679.2:g.41769190C>T | GRCh38 |
| NC_000017.10:g.39925442C>T , CM000679.1:g.39925442C>T | GRCh37 |
| NC_000017.9:g.37178968C>T | NCBI36 |
| NG_009090.2:g.22523G>A , LRG_401:g.22523G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000393931.8:c.486G>A MANE Select | ENSP00000377508.3:p.Ala162= | |
| ENST00000310706.9:c.486G>A | ENSP00000311113.5:p.Ala162= | |
| ENST00000393930.5:c.486G>A | ENSP00000377507.1:p.Ala162= | |
| ENST00000393931.7:c.486G>A | ENSP00000377508.3:p.Ala162= | |
| ENST00000420370.5:c.486G>A | ENSP00000411449.1:p.Ala162= | |
| ENST00000424457.5:c.486G>A | ENSP00000401034.1:p.Ala162= | |
| ENST00000437187.5:c.486G>A | ENSP00000394146.1:p.Ala162= | |
| ENST00000449889.5:c.486G>A | ENSP00000389886.1:p.Ala162= | |
| NM_002230.2:c.486G>A , LRG_401t2:c.486G>A | NP_002221.1:p.Ala162= | |
| NM_021991.2:c.486G>A , LRG_401t1:c.486G>A | NP_068831.1:p.Ala162= | |
| XM_006721873.1:c.486G>A | XP_006721936.1:p.Ala162= | |
| XM_006721874.1:c.486G>A | XP_006721937.1:p.Ala162= | |
| XM_006721875.1:c.486G>A | XP_006721938.1:p.Ala162= | |
| XM_006721878.1:c.486G>A | XP_006721941.1:p.Ala162= | |
| XM_011524753.1:c.486G>A | XP_011523055.1:p.Ala162= | |
| XM_011524754.1:c.486G>A | XP_011523056.1:p.Ala162= | |
| XM_011524755.1:c.486G>A | XP_011523057.1:p.Ala162= | |
| XM_011524756.1:c.486G>A | XP_011523058.1:p.Ala162= | |
| XM_011524757.1:c.486G>A | XP_011523059.1:p.Ala162= | |
| XM_011524758.1:c.486G>A | XP_011523060.1:p.Ala162= | |
| NM_001352773.1:c.486G>A | NP_001339702.1:p.Ala162= | |
| NM_001352774.1:c.486G>A | NP_001339703.1:p.Ala162= | |
| NM_001352775.1:c.486G>A | NP_001339704.1:p.Ala162= | |
| NM_001352776.1:c.486G>A | NP_001339705.1:p.Ala162= | |
| NM_001352777.1:c.486G>A | NP_001339706.1:p.Ala162= | |
| NM_002230.3:c.486G>A | NP_002221.1:p.Ala162= | |
| NM_021991.3:c.486G>A | NP_068831.1:p.Ala162= | |
| XM_006721874.3:c.486G>A | XP_006721937.1:p.Ala162= | |
| XM_011524753.2:c.486G>A | XP_011523055.1:p.Ala162= | |
| XM_017024588.2:c.537G>A | XP_016880077.1:p.Ala179= | |
| XM_017024590.1:c.486G>A | XP_016880079.1:p.Ala162= | |
| NM_002230.4:c.486G>A MANE Select | NP_002221.1:p.Ala162= | |
| NM_001352773.2:c.486G>A | NP_001339702.1:p.Ala162= | |
| NM_001352774.2:c.486G>A | NP_001339703.1:p.Ala162= | |
| NM_001352775.2:c.486G>A | NP_001339704.1:p.Ala162= | |
| NM_001352776.2:c.486G>A | NP_001339705.1:p.Ala162= | |
| NM_001352777.2:c.486G>A | NP_001339706.1:p.Ala162= | |
| NM_021991.4:c.486G>A | NP_068831.1:p.Ala162= |