Linked Data
ClinVar Variation Id:
406731
dbSNP Id:
rs876660325
gnomAD v3:
2-214767503-T-C
gnomAD v4:
2-214767503-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.214767503T>C , CM000664.2:g.214767503T>C | GRCh38 |
| NC_000002.11:g.215632227T>C , CM000664.1:g.215632227T>C | GRCh37 |
| NC_000002.10:g.215340472T>C | NCBI36 |
| NG_012047.2:g.47202A>G | |
| NG_012047.3:g.47209A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260947.9:c.1547A>G MANE Select | ENSP00000260947.4:p.Tyr516Cys | |
| ENST00000421162.2:c.216-14948A>G | ENSP00000392245.2:n.216-14948A>G | |
| ENST00000613192.2:c.159-36995A>G | ENSP00000483275.2:n.159-36995A>G | |
| ENST00000613374.5:c.159-14948A>G | ENSP00000484464.1:n.159-14948A>G | |
| ENST00000613706.5:c.1139A>G | ENSP00000484976.2:p.Tyr380Cys | |
| ENST00000617164.5:c.1490A>G | ENSP00000480470.1:p.Tyr497Cys | |
| ENST00000619009.5:c.364+24794A>G | ENSP00000482293.1:n.364+24794A>G | |
| ENST00000650978.1:c.2922A>G | ||
| ENST00000260947.8:c.1547A>G | ENSP00000260947.4:p.Tyr516Cys | |
| ENST00000421162.1:c.216-14948A>G | ENSP00000392245.1:n.216-14948A>G | |
| ENST00000455743.5:c.*1167A>G | ENSP00000412186.1:n.*1167A>G | |
| ENST00000613192.1:c.74-36995A>G | ENSP00000483275.1:n.74-36995A>G | |
| ENST00000613374.4:c.159-14948A>G | ENSP00000484464.1:n.159-14948A>G | |
| ENST00000613706.4:c.216-14948A>G | ENSP00000484976.1:n.216-14948A>G | |
| ENST00000617164.4:c.1490A>G | ENSP00000480470.1:p.Tyr497Cys | |
| ENST00000619009.4:c.364+24794A>G | ENSP00000482293.1:n.364+24794A>G | |
| ENST00000620057.4:c.*213A>G | ENSP00000481988.1:n.*213A>G | |
| NM_000465.3:c.1547A>G | NP_000456.2:p.Tyr516Cys | |
| NM_001282543.1:c.1490A>G | NP_001269472.1:p.Tyr497Cys | |
| NM_001282545.1:c.216-14948A>G | NP_001269474.1:n.216-14948A>G | |
| NM_001282548.1:c.159-14948A>G | NP_001269477.1:n.159-14948A>G | |
| NM_001282549.1:c.364+24794A>G | NP_001269478.1:n.364+24794A>G | |
| NR_104212.1:n.1540A>G | ||
| NR_104215.1:n.1483A>G | ||
| NR_104216.1:n.739A>G | ||
| XM_011511567.1:c.1493A>G | XP_011509869.1:p.Tyr498Cys | |
| XM_011511568.1:c.1547A>G | XP_011509870.1:p.Tyr516Cys | |
| XM_017004613.1:c.1646A>G | XP_016860102.1:p.Tyr549Cys | |
| XM_017004614.1:c.1646A>G | XP_016860103.1:p.Tyr549Cys | |
| XR_002959322.1:n.1737A>G | ||
| NM_000465.4:c.1547A>G MANE Select | NP_000456.2:p.Tyr516Cys | |
| NM_001282543.2:c.1490A>G | NP_001269472.1:p.Tyr497Cys | |
| NM_001282545.2:c.216-14948A>G | NP_001269474.1:n.216-14948A>G | |
| NM_001282548.2:c.159-14948A>G | NP_001269477.1:n.159-14948A>G | |
| NM_001282549.2:c.364+24794A>G | NP_001269478.1:n.364+24794A>G | |
| NR_104212.2:n.1512A>G | ||
| NR_104215.2:n.1455A>G | ||
| NR_104216.2:n.711A>G |