Linked Data
ClinVar Variation Id:
45879
dbSNP Id:
rs199508694
ExAC:
10:73437335 G / A
gnomAD v2:
10-73437335-G-A
gnomAD v3:
10-71677578-G-A
gnomAD v4:
10-71677578-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.71677578G>A , CM000672.2:g.71677578G>A | GRCh38 |
| NC_000010.10:g.73437335G>A , CM000672.1:g.73437335G>A | GRCh37 |
| NC_000010.9:g.73107341G>A | NCBI36 |
| NG_008835.1:g.285632G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000224721.12:c.1637G>A MANE Select | ENSP00000224721.9:p.Arg546Gln | |
| ENST00000398809.9:c.1637G>A | ENSP00000381789.5:p.Arg546Gln | |
| ENST00000442677.4:c.1637G>A | ENSP00000388894.3:p.Arg546Gln | |
| ENST00000466757.8:c.1068G>A | ||
| ENST00000224721.10:c.1652G>A | ENSP00000224721.8:p.Arg551Gln | |
| ENST00000299366.11:c.1637G>A | ENSP00000299366.8:p.Arg546Gln | |
| ENST00000398809.8:c.1637G>A | ENSP00000381789.5:p.Arg546Gln | |
| ENST00000442677.3:c.412G>A | ||
| ENST00000466757.7:c.1068G>A | ||
| ENST00000616684.4:c.1637G>A | ENSP00000482036.2:p.Arg546Gln | |
| ENST00000622827.4:c.1637G>A | ENSP00000483211.1:p.Arg546Gln | |
| NM_001171930.1:c.1637G>A | NP_001165401.1:p.Arg546Gln | |
| NM_001171931.1:c.1637G>A | NP_001165402.1:p.Arg546Gln | |
| NM_022124.5:c.1637G>A | NP_071407.4:p.Arg546Gln | |
| XM_006717940.2:c.1832G>A | XP_006718003.1:p.Arg611Gln | |
| XM_006717942.2:c.1766G>A | XP_006718005.1:p.Arg589Gln | |
| XM_011540039.1:c.1832G>A | XP_011538341.1:p.Arg611Gln | |
| XM_011540040.1:c.1826G>A | XP_011538342.1:p.Arg609Gln | |
| XM_011540041.1:c.1772G>A | XP_011538343.1:p.Arg591Gln | |
| XM_011540042.1:c.1832G>A | XP_011538344.1:p.Arg611Gln | |
| XM_011540043.1:c.1832G>A | XP_011538345.1:p.Arg611Gln | |
| XM_011540044.1:c.1697G>A | XP_011538346.1:p.Arg566Gln | |
| XM_011540045.1:c.1832G>A | XP_011538347.1:p.Arg611Gln | |
| XM_011540046.1:c.1292G>A | XP_011538348.1:p.Arg431Gln | |
| XM_011540047.1:c.650G>A | XP_011538349.1:p.Arg217Gln | |
| XM_011540048.1:c.1832G>A | XP_011538350.1:p.Arg611Gln | |
| XM_011540049.1:c.1832G>A | XP_011538351.1:p.Arg611Gln | |
| XM_011540050.1:c.1832G>A | XP_011538352.1:p.Arg611Gln | |
| XM_011540051.1:c.1832G>A | XP_011538353.1:p.Arg611Gln | |
| XM_011540053.1:c.1832G>A | XP_011538355.1:p.Arg611Gln | |
| XM_011540054.1:c.1772G>A | XP_011538356.1:p.Arg591Gln | |
| XR_945796.1:n.2075G>A | ||
| NM_001171930.2:c.1637G>A | NP_001165401.1:p.Arg546Gln | |
| NM_001171931.2:c.1637G>A | NP_001165402.1:p.Arg546Gln | |
| NM_022124.6:c.1637G>A MANE Select | NP_071407.4:p.Arg546Gln |