Linked Data
ClinVar Variation Id:
8300
ClinVar RCV Id:
RCV000008798
dbSNP Id:
rs267606681
gnomAD v4:
2-127068982-C-T
PubMed:
PMID:20142620
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.127068982C>T , CM000664.2:g.127068982C>T | GRCh38 |
| NC_000002.11:g.127826558C>T , CM000664.1:g.127826558C>T | GRCh37 |
| NC_000002.10:g.127543028C>T | NCBI36 |
| NG_012042.1:g.43307G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000352848.8:c.461G>A | ENSP00000315284.4:p.Arg154Gln | |
| ENST00000316724.10:c.461G>A MANE Select | ENSP00000316779.5:p.Arg154Gln | |
| ENST00000259238.8:c.461G>A | ENSP00000259238.4:p.Arg154Gln | |
| ENST00000316724.9:c.461G>A | ENSP00000316779.5:p.Arg154Gln | |
| ENST00000346226.7:c.461G>A | ENSP00000315411.3:p.Arg154Gln | |
| ENST00000348750.8:c.461G>A | ENSP00000259237.5:p.Arg154Gln | |
| ENST00000351659.7:c.461G>A | ENSP00000315388.3:p.Arg154Gln | |
| ENST00000352848.7:c.461G>A | ENSP00000315284.4:p.Arg154Gln | |
| ENST00000357970.7:c.461G>A | ENSP00000350654.3:p.Arg154Gln | |
| ENST00000376113.6:c.461G>A | ENSP00000365281.2:p.Arg154Gln | |
| ENST00000393040.7:c.461G>A | ENSP00000376760.3:p.Arg154Gln | |
| ENST00000393041.7:c.461G>A | ENSP00000376761.3:p.Arg154Gln | |
| ENST00000409400.1:c.461G>A | ENSP00000386797.1:p.Arg154Gln | |
| NM_004305.3:c.461G>A | NP_004296.1:p.Arg154Gln | |
| NM_139343.2:c.461G>A | NP_647593.1:p.Arg154Gln | |
| NM_139344.2:c.461G>A | NP_647594.1:p.Arg154Gln | |
| NM_139345.2:c.461G>A | NP_647595.1:p.Arg154Gln | |
| NM_139346.2:c.461G>A | NP_647596.1:p.Arg154Gln | |
| NM_139347.2:c.461G>A | NP_647597.1:p.Arg154Gln | |
| NM_139348.2:c.461G>A | NP_647598.1:p.Arg154Gln | |
| NM_139349.2:c.461G>A | NP_647599.1:p.Arg154Gln | |
| NM_139350.2:c.461G>A | NP_647600.1:p.Arg154Gln | |
| NM_139351.2:c.461G>A | NP_647601.1:p.Arg154Gln | |
| XM_005263642.2:c.461G>A | XP_005263699.1:p.Arg154Gln | |
| XM_005263643.2:c.461G>A | XP_005263700.1:p.Arg154Gln | |
| XM_005263644.2:c.461G>A | XP_005263701.1:p.Arg154Gln | |
| XM_005263645.1:c.389G>A | XP_005263702.1:p.Arg130Gln | |
| XM_005263646.2:c.461G>A | XP_005263703.1:p.Arg154Gln | |
| XM_005263647.2:c.461G>A | XP_005263704.1:p.Arg154Gln | |
| XM_005263648.1:c.389G>A | XP_005263705.1:p.Arg130Gln | |
| XM_006712425.2:c.461G>A | XP_006712488.1:p.Arg154Gln | |
| XM_006712426.2:c.461G>A | XP_006712489.1:p.Arg154Gln | |
| XM_006712427.1:c.389G>A | XP_006712490.1:p.Arg130Gln | |
| XM_006712428.2:c.461G>A | XP_006712491.1:p.Arg154Gln | |
| XM_006712429.2:c.461G>A | XP_006712492.1:p.Arg154Gln | |
| XM_006712430.2:c.461G>A | XP_006712493.1:p.Arg154Gln | |
| XM_006712431.2:c.461G>A | XP_006712494.1:p.Arg154Gln | |
| XM_006712432.2:c.461G>A | XP_006712495.1:p.Arg154Gln | |
| XM_006712433.2:c.461G>A | XP_006712496.1:p.Arg154Gln | |
| XM_006712434.2:c.461G>A | XP_006712497.1:p.Arg154Gln | |
| XM_011510975.1:c.380G>A | XP_011509277.1:p.Arg127Gln | |
| NM_001320632.1:c.461G>A | NP_001307561.1:p.Arg154Gln | |
| NM_001320633.1:c.461G>A | NP_001307562.1:p.Arg154Gln | |
| NM_001320634.1:c.389G>A | NP_001307563.1:p.Arg130Gln | |
| NM_001320640.1:c.461G>A | NP_001307569.1:p.Arg154Gln | |
| NM_001320641.1:c.461G>A | NP_001307570.1:p.Arg154Gln | |
| NM_001320642.1:c.380G>A | NP_001307571.1:p.Arg127Gln | |
| XM_005263642.4:c.461G>A | XP_005263699.1:p.Arg154Gln | |
| XM_005263643.4:c.461G>A | XP_005263700.1:p.Arg154Gln | |
| XM_005263645.2:c.389G>A | XP_005263702.1:p.Arg130Gln | |
| XM_006712425.4:c.461G>A | XP_006712488.1:p.Arg154Gln | |
| XM_006712426.4:c.461G>A | XP_006712489.1:p.Arg154Gln | |
| XM_006712427.2:c.389G>A | XP_006712490.1:p.Arg130Gln | |
| XM_006712428.4:c.461G>A | XP_006712491.1:p.Arg154Gln | |
| XM_006712429.4:c.461G>A | XP_006712492.1:p.Arg154Gln | |
| XM_006712431.4:c.461G>A | XP_006712494.1:p.Arg154Gln | |
| XM_006712432.4:c.461G>A | XP_006712495.1:p.Arg154Gln | |
| XM_006712433.4:c.461G>A | XP_006712496.1:p.Arg154Gln | |
| XM_006712434.4:c.461G>A | XP_006712497.1:p.Arg154Gln | |
| XM_011510975.3:c.380G>A | XP_011509277.1:p.Arg127Gln | |
| XM_017003819.1:c.389G>A | XP_016859308.1:p.Arg130Gln | |
| XM_017003820.2:c.461G>A | XP_016859309.1:p.Arg154Gln | |
| XM_017003821.2:c.461G>A | XP_016859310.1:p.Arg154Gln | |
| XM_017003822.2:c.461G>A | XP_016859311.1:p.Arg154Gln | |
| XM_017003823.1:c.389G>A | XP_016859312.1:p.Arg130Gln | |
| XM_017003824.1:c.389G>A | XP_016859313.1:p.Arg130Gln | |
| XM_017003825.1:c.389G>A | XP_016859314.1:p.Arg130Gln | |
| XM_017003826.1:c.389G>A | XP_016859315.1:p.Arg130Gln | |
| XM_017003827.2:c.461G>A | XP_016859316.1:p.Arg154Gln | |
| XM_017003828.2:c.461G>A | XP_016859317.1:p.Arg154Gln | |
| NM_139343.3:c.461G>A MANE Select | NP_647593.1:p.Arg154Gln | |
| NM_001320632.2:c.461G>A | NP_001307561.1:p.Arg154Gln | |
| NM_001320633.2:c.461G>A | NP_001307562.1:p.Arg154Gln | |
| NM_001320640.2:c.461G>A | NP_001307569.1:p.Arg154Gln | |
| NM_001320641.2:c.461G>A | NP_001307570.1:p.Arg154Gln | |
| NM_004305.4:c.461G>A | NP_004296.1:p.Arg154Gln | |
| NM_139344.3:c.461G>A | NP_647594.1:p.Arg154Gln | |
| NM_139345.3:c.461G>A | NP_647595.1:p.Arg154Gln | |
| NM_139346.3:c.461G>A | NP_647596.1:p.Arg154Gln | |
| NM_139347.3:c.461G>A | NP_647597.1:p.Arg154Gln | |
| NM_139348.3:c.461G>A | NP_647598.1:p.Arg154Gln | |
| NM_139349.3:c.461G>A | NP_647599.1:p.Arg154Gln | |
| NM_139350.3:c.461G>A | NP_647600.1:p.Arg154Gln | |
| NM_139351.3:c.461G>A | NP_647601.1:p.Arg154Gln |