Linked Data
ClinVar Variation Id:
230520
dbSNP Id:
rs754122018
gnomAD v3:
5-112840632-C-T
gnomAD v4:
5-112840632-C-T
PubMed:
PMID:12494469
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112840632C>T , CM000667.2:g.112840632C>T | GRCh38 |
| NC_000005.9:g.112176329C>T , CM000667.1:g.112176329C>T | GRCh37 |
| NC_000005.8:g.112204228C>T | NCBI36 |
| NG_008481.4:g.153112C>T , LRG_130:g.153112C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504915.3:c.5092C>T | ENSP00000473355.2:p.Gln1698Ter | |
| ENST00000505350.2:c.*5044C>T | ENSP00000481752.1:n.*5044C>T | |
| ENST00000507379.6:c.4984C>T | ENSP00000423224.2:p.Gln1662Ter | |
| ENST00000509732.6:c.5038C>T | ENSP00000426541.2:p.Gln1680Ter | |
| ENST00000512211.7:c.5038C>T | ENSP00000423828.3:p.Gln1680Ter | |
| ENST00000257430.9:c.5038C>T MANE Select | ENSP00000257430.4:p.Gln1680Ter | |
| ENST00000257430.8:c.5038C>T | ENSP00000257430.4:p.Gln1680Ter | |
| ENST00000508376.6:c.5038C>T | ENSP00000427089.2:p.Gln1680Ter | |
| ENST00000508624.5:c.*4360C>T | ENSP00000424265.1:n.*4360C>T | |
| ENST00000520401.1:c.230+11660C>T | ||
| NM_000038.5:c.5038C>T | NP_000029.2:p.Gln1680Ter | |
| NM_001127510.2:c.5038C>T | NP_001120982.1:p.Gln1680Ter | |
| NM_001127511.2:c.4984C>T | NP_001120983.2:p.Gln1662Ter | |
| NM_001354895.1:c.5038C>T | NP_001341824.1:p.Gln1680Ter | |
| NM_001354896.1:c.5092C>T | NP_001341825.1:p.Gln1698Ter | |
| NM_001354897.1:c.5068C>T | NP_001341826.1:p.Gln1690Ter | |
| NM_001354898.1:c.4963C>T | NP_001341827.1:p.Gln1655Ter | |
| NM_001354899.1:c.4954C>T | NP_001341828.1:p.Gln1652Ter | |
| NM_001354900.1:c.4915C>T | NP_001341829.1:p.Gln1639Ter | |
| NM_001354901.1:c.4861C>T | NP_001341830.1:p.Gln1621Ter | |
| NM_001354902.1:c.4765C>T | NP_001341831.1:p.Gln1589Ter | |
| NM_001354903.1:c.4735C>T | NP_001341832.1:p.Gln1579Ter | |
| NM_001354904.1:c.4660C>T | NP_001341833.1:p.Gln1554Ter | |
| NM_001354905.1:c.4558C>T | NP_001341834.1:p.Gln1520Ter | |
| NM_001354906.1:c.4189C>T | NP_001341835.1:p.Gln1397Ter | |
| NM_000038.6:c.5038C>T MANE Select | NP_000029.2:p.Gln1680Ter | |
| NM_001127510.3:c.5038C>T | NP_001120982.1:p.Gln1680Ter | |
| NM_001127511.3:c.4984C>T | NP_001120983.2:p.Gln1662Ter | |
| NM_001354895.2:c.5038C>T | NP_001341824.1:p.Gln1680Ter | |
| NM_001354896.2:c.5092C>T | NP_001341825.1:p.Gln1698Ter | |
| NM_001354897.2:c.5068C>T | NP_001341826.1:p.Gln1690Ter | |
| NM_001354898.2:c.4963C>T | NP_001341827.1:p.Gln1655Ter | |
| NM_001354899.2:c.4954C>T | NP_001341828.1:p.Gln1652Ter | |
| NM_001354900.2:c.4915C>T | NP_001341829.1:p.Gln1639Ter | |
| NM_001354901.2:c.4861C>T | NP_001341830.1:p.Gln1621Ter | |
| NM_001354902.2:c.4765C>T | NP_001341831.1:p.Gln1589Ter | |
| NM_001354903.2:c.4735C>T | NP_001341832.1:p.Gln1579Ter | |
| NM_001354904.2:c.4660C>T | NP_001341833.1:p.Gln1554Ter | |
| NM_001354905.2:c.4558C>T | NP_001341834.1:p.Gln1520Ter | |
| NM_001354906.2:c.4189C>T | NP_001341835.1:p.Gln1397Ter |