Linked Data
ClinVar Variation Id:
335256
dbSNP Id:
rs191428830
ExAC:
2:241659323 C / T
gnomAD v2:
2-241659323-C-T
gnomAD v3:
2-240719906-C-T
gnomAD v4:
2-240719906-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240719906C>T , CM000664.2:g.240719906C>T | GRCh38 |
| NC_000002.11:g.241659323C>T , CM000664.1:g.241659323C>T | GRCh37 |
| NC_000002.10:g.241307996C>T | NCBI36 |
| NG_029724.1:g.105302G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320389.12:c.4610G>A | ENSP00000322791.8:p.Arg1537Gln | |
| ENST00000404283.9:c.4913G>A | ENSP00000384231.5:p.Arg1638Gln | |
| ENST00000431776.6:c.1709G>A | ENSP00000414613.2:p.Arg570Gln | |
| ENST00000492812.6:n.3472G>A | ||
| ENST00000498729.9:c.4889G>A MANE Select | ENSP00000438388.1:p.Arg1630Gln | |
| ENST00000647731.1:c.4613G>A | ENSP00000498099.1:p.Arg1538Gln | |
| ENST00000647885.1:c.4700G>A | ENSP00000497739.1:p.Arg1567Gln | |
| ENST00000648047.1:c.3848G>A | ENSP00000497935.1:p.Arg1283Gln | |
| ENST00000648129.1:c.4862G>A | ENSP00000497293.1:p.Arg1621Gln | |
| ENST00000648364.1:c.4613G>A | ENSP00000498196.1:p.Arg1538Gln | |
| ENST00000648680.1:c.4640G>A | ENSP00000497586.1:p.Arg1547Gln | |
| ENST00000649096.1:c.4586G>A | ENSP00000497030.1:p.Arg1529Gln | |
| ENST00000649190.1:n.3883G>A | ||
| ENST00000649306.1:c.4688G>A | ENSP00000497678.1:p.Arg1563Gln | |
| ENST00000650053.1:c.4586G>A | ENSP00000497824.1:p.Arg1529Gln | |
| ENST00000650130.1:c.4862G>A | ENSP00000498082.1:p.Arg1621Gln | |
| ENST00000650430.1:n.3961G>A | ||
| ENST00000675644.1:c.311G>A | ENSP00000502435.1:n.311G>A | |
| ENST00000675932.1:c.166G>A | ENSP00000502786.1:p.Gly56Ser | |
| ENST00000320389.11:c.4586G>A | ENSP00000322791.7:p.Arg1529Gln | |
| ENST00000460788.5:n.1446G>A | ||
| ENST00000488776.1:n.380G>A | ||
| ENST00000492812.5:n.1361G>A | ||
| ENST00000498729.6:c.4889G>A | ENSP00000438388.1:p.Arg1630Gln | |
| NM_001244008.1:c.4889G>A | NP_001230937.1:p.Arg1630Gln | |
| NM_004321.6:c.4586G>A | NP_004312.2:p.Arg1529Gln | |
| XM_005247022.1:c.4916G>A | XP_005247079.1:p.Arg1639Gln | |
| XM_005247023.1:c.4913G>A | XP_005247080.1:p.Arg1638Gln | |
| XM_005247024.1:c.4889G>A | XP_005247081.1:p.Arg1630Gln | |
| XM_005247026.1:c.4613G>A | XP_005247083.1:p.Arg1538Gln | |
| XM_005247027.1:c.4610G>A | XP_005247084.1:p.Arg1537Gln | |
| XM_005247028.1:c.4586G>A | XP_005247085.1:p.Arg1529Gln | |
| XM_006712605.1:c.4862G>A | XP_006712668.1:p.Arg1621Gln | |
| XM_011511364.1:c.4916G>A | XP_011509666.1:p.Arg1639Gln | |
| XM_011511365.1:c.4640G>A | XP_011509667.1:p.Arg1547Gln | |
| XM_011511366.1:c.3911G>A | XP_011509668.1:p.Arg1304Gln | |
| XM_011511367.1:c.3911G>A | XP_011509669.1:p.Arg1304Gln | |
| NM_001320705.1:c.4613G>A | NP_001307634.1:p.Arg1538Gln | |
| NM_001330289.1:c.4640G>A | NP_001317218.1:p.Arg1547Gln | |
| NM_001330290.1:c.4688G>A | NP_001317219.1:p.Arg1563Gln | |
| NM_004321.7:c.4586G>A | NP_004312.2:p.Arg1529Gln | |
| NM_001320705.2:c.4613G>A | NP_001307634.1:p.Arg1538Gln | |
| NM_001330289.2:c.4640G>A | NP_001317218.1:p.Arg1547Gln | |
| NM_001330290.2:c.4688G>A | NP_001317219.1:p.Arg1563Gln | |
| NM_001244008.2:c.4889G>A MANE Select | NP_001230937.1:p.Arg1630Gln | |
| NM_001379631.1:c.4964G>A | NP_001366560.1:p.Arg1655Gln | |
| NM_001379632.1:c.4865G>A | NP_001366561.1:p.Arg1622Gln | |
| NM_001379633.1:c.4862G>A | NP_001366562.1:p.Arg1621Gln | |
| NM_001379634.1:c.4715G>A | NP_001366563.1:p.Arg1572Gln | |
| NM_001379635.1:c.4712G>A | NP_001366564.1:p.Arg1571Gln | |
| NM_001379636.1:c.4700G>A | NP_001366565.1:p.Arg1567Gln | |
| NM_001379637.1:c.4661G>A | NP_001366566.1:p.Arg1554Gln | |
| NM_001379638.1:c.4637G>A | NP_001366567.1:p.Arg1546Gln | |
| NM_001379639.1:c.4610G>A | NP_001366568.1:p.Arg1537Gln | |
| NM_001379640.1:c.4583G>A | NP_001366569.1:p.Arg1528Gln | |
| NM_001379641.1:c.4586G>A | NP_001366570.1:p.Arg1529Gln | |
| NM_001379642.1:c.4889G>A | NP_001366571.1:p.Arg1630Gln | |
| NM_001379645.1:c.4862G>A | NP_001366574.1:p.Arg1621Gln | |
| NM_001379646.1:c.4712G>A | NP_001366575.1:p.Arg1571Gln | |
| NM_001379648.1:c.4688G>A | NP_001366577.1:p.Arg1563Gln | |
| NM_001379649.1:c.4613G>A | NP_001366578.1:p.Arg1538Gln | |
| NM_001379650.1:c.4586G>A | NP_001366579.1:p.Arg1529Gln | |
| NM_001379651.1:c.4586G>A | NP_001366580.1:p.Arg1529Gln | |
| NM_001379653.1:c.4586G>A | NP_001366582.1:p.Arg1529Gln | |
| NM_004321.8:c.4586G>A | NP_004312.2:p.Arg1529Gln |