Linked Data
ClinVar Variation Id:
411364
dbSNP Id:
rs369345931
ExAC:
5:112137037 A / G
gnomAD v2:
5-112137037-A-G
gnomAD v3:
5-112801340-A-G
gnomAD v4:
5-112801340-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112801340A>G , CM000667.2:g.112801340A>G | GRCh38 |
| NC_000005.9:g.112137037A>G , CM000667.1:g.112137037A>G | GRCh37 |
| NC_000005.8:g.112164936A>G | NCBI36 |
| NG_008481.4:g.113820A>G , LRG_130:g.113820A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.791A>G | ENSP00000484935.2:p.Gln264Arg | |
| ENST00000504915.3:c.791A>G | ENSP00000473355.2:p.Gln264Arg | |
| ENST00000505084.2:n.847A>G | ||
| ENST00000505350.2:c.*797A>G | ENSP00000481752.1:n.*797A>G | |
| ENST00000507379.6:c.737A>G | ENSP00000423224.2:p.Gln246Arg | |
| ENST00000509732.6:c.791A>G | ENSP00000426541.2:p.Gln264Arg | |
| ENST00000512211.7:c.791A>G | ENSP00000423828.3:p.Gln264Arg | |
| ENST00000257430.9:c.791A>G MANE Select | ENSP00000257430.4:p.Gln264Arg | |
| ENST00000257430.8:c.791A>G | ENSP00000257430.4:p.Gln264Arg | |
| ENST00000507379.5:c.737A>G | ENSP00000423224.1:p.Gln246Arg | |
| ENST00000508376.6:c.791A>G | ENSP00000427089.2:p.Gln264Arg | |
| ENST00000508624.5:c.791A>G | ENSP00000424265.1:p.Gln264Arg | |
| ENST00000512211.6:c.791A>G | ENSP00000423828.2:p.Gln264Arg | |
| NM_000038.5:c.791A>G | NP_000029.2:p.Gln264Arg | |
| NM_001127510.2:c.791A>G | NP_001120982.1:p.Gln264Arg | |
| NM_001127511.2:c.737A>G | NP_001120983.2:p.Gln246Arg | |
| NM_001354895.1:c.791A>G | NP_001341824.1:p.Gln264Arg | |
| NM_001354896.1:c.791A>G | NP_001341825.1:p.Gln264Arg | |
| NM_001354897.1:c.821A>G | NP_001341826.1:p.Gln274Arg | |
| NM_001354898.1:c.716A>G | NP_001341827.1:p.Gln239Arg | |
| NM_001354899.1:c.707A>G | NP_001341828.1:p.Gln236Arg | |
| NM_001354900.1:c.614A>G | NP_001341829.1:p.Gln205Arg | |
| NM_001354901.1:c.614A>G | NP_001341830.1:p.Gln205Arg | |
| NM_001354902.1:c.821A>G | NP_001341831.1:p.Gln274Arg | |
| NM_001354903.1:c.791A>G | NP_001341832.1:p.Gln264Arg | |
| NM_001354904.1:c.716A>G | NP_001341833.1:p.Gln239Arg | |
| NM_001354905.1:c.614A>G | NP_001341834.1:p.Gln205Arg | |
| NM_001354906.1:c.-245A>G | NP_001341835.1:n.-245A>G | |
| NM_000038.6:c.791A>G MANE Select | NP_000029.2:p.Gln264Arg | |
| NM_001127510.3:c.791A>G | NP_001120982.1:p.Gln264Arg | |
| NM_001127511.3:c.737A>G | NP_001120983.2:p.Gln246Arg | |
| NM_001354895.2:c.791A>G | NP_001341824.1:p.Gln264Arg | |
| NM_001354896.2:c.791A>G | NP_001341825.1:p.Gln264Arg | |
| NM_001354897.2:c.821A>G | NP_001341826.1:p.Gln274Arg | |
| NM_001354898.2:c.716A>G | NP_001341827.1:p.Gln239Arg | |
| NM_001354899.2:c.707A>G | NP_001341828.1:p.Gln236Arg | |
| NM_001354900.2:c.614A>G | NP_001341829.1:p.Gln205Arg | |
| NM_001354901.2:c.614A>G | NP_001341830.1:p.Gln205Arg | |
| NM_001354902.2:c.821A>G | NP_001341831.1:p.Gln274Arg | |
| NM_001354903.2:c.791A>G | NP_001341832.1:p.Gln264Arg | |
| NM_001354904.2:c.716A>G | NP_001341833.1:p.Gln239Arg | |
| NM_001354905.2:c.614A>G | NP_001341834.1:p.Gln205Arg | |
| NM_001354906.2:c.-245A>G | NP_001341835.1:n.-245A>G |