Linked Data
ClinVar Variation Id:
45977
dbSNP Id:
rs376271562
ExAC:
10:73544085 C / T
gnomAD v2:
10-73544085-C-T
gnomAD v3:
10-71784328-C-T
gnomAD v4:
10-71784328-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.71784328C>T , CM000672.2:g.71784328C>T | GRCh38 |
| NC_000010.10:g.73544085C>T , CM000672.1:g.73544085C>T | GRCh37 |
| NC_000010.9:g.73214091C>T | NCBI36 |
| NG_008835.1:g.392382C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000224721.12:c.5410C>T MANE Select | ENSP00000224721.9:p.Arg1804Trp | |
| ENST00000224721.10:c.5425C>T | ENSP00000224721.8:p.Arg1809Trp | |
| ENST00000622827.4:c.5410C>T | ENSP00000483211.1:p.Arg1804Trp | |
| NM_022124.5:c.5410C>T | NP_071407.4:p.Arg1804Trp | |
| XM_006717940.2:c.5605C>T | XP_006718003.1:p.Arg1869Trp | |
| XM_006717942.2:c.5539C>T | XP_006718005.1:p.Arg1847Trp | |
| XM_011540039.1:c.5602C>T | XP_011538341.1:p.Arg1868Trp | |
| XM_011540040.1:c.5599C>T | XP_011538342.1:p.Arg1867Trp | |
| XM_011540041.1:c.5545C>T | XP_011538343.1:p.Arg1849Trp | |
| XM_011540042.1:c.5605C>T | XP_011538344.1:p.Arg1869Trp | |
| XM_011540043.1:c.5605C>T | XP_011538345.1:p.Arg1869Trp | |
| XM_011540044.1:c.5470C>T | XP_011538346.1:p.Arg1824Trp | |
| XM_011540045.1:c.5605C>T | XP_011538347.1:p.Arg1869Trp | |
| XM_011540046.1:c.5065C>T | XP_011538348.1:p.Arg1689Trp | |
| XM_011540047.1:c.4423C>T | XP_011538349.1:p.Arg1475Trp | |
| XM_011540048.1:c.5605C>T | XP_011538350.1:p.Arg1869Trp | |
| XM_011540049.1:c.5605C>T | XP_011538351.1:p.Arg1869Trp | |
| XM_011540050.1:c.5605C>T | XP_011538352.1:p.Arg1869Trp | |
| XM_011540051.1:c.5605C>T | XP_011538353.1:p.Arg1869Trp | |
| XM_011540052.1:c.1933C>T | XP_011538354.1:p.Arg645Trp | |
| XM_011540053.1:c.5605C>T | XP_011538355.1:p.Arg1869Trp | |
| XR_945796.1:n.5848C>T | ||
| NM_022124.6:c.5410C>T MANE Select | NP_071407.4:p.Arg1804Trp |