Linked Data
ClinVar Variation Id:
312642
dbSNP Id:
rs149753029
ExAC:
14:102493523 A / G
gnomAD v2:
14-102493523-A-G
gnomAD v3:
14-102027186-A-G
gnomAD v4:
14-102027186-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.102027186A>G , CM000676.2:g.102027186A>G | GRCh38 |
| NC_000014.8:g.102493523A>G , CM000676.1:g.102493523A>G | GRCh37 |
| NC_000014.7:g.101563276A>G | NCBI36 |
| NG_008777.1:g.67659A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000684561.1:c.*243A>G | ENSP00000506816.1:n.*243A>G | |
| ENST00000360184.10:c.8784A>G MANE Select | ENSP00000348965.4:p.Gln2928= | |
| ENST00000643508.2:c.8784A>G | ENSP00000495528.2:p.Gln2928= | |
| ENST00000644881.2:c.8784A>G | ENSP00000495022.2:p.Gln2928= | |
| ENST00000645039.2:c.8784A>G | ENSP00000495220.2:p.Gln2928= | |
| ENST00000645149.2:c.8784A>G | ENSP00000495944.2:p.Gln2928= | |
| ENST00000647119.1:n.239A>G | ||
| ENST00000647366.1:n.2338A>G | ||
| ENST00000679486.1:c.8784A>G | ENSP00000506688.1:p.Gln2928= | |
| ENST00000679629.1:c.8784A>G | ENSP00000505589.1:p.Gln2928= | |
| ENST00000679720.1:c.8784A>G | ENSP00000505938.1:p.Gln2928= | |
| ENST00000679910.1:c.8784A>G | ENSP00000506521.1:p.Gln2928= | |
| ENST00000680120.1:c.8784A>G | ENSP00000504863.1:p.Gln2928= | |
| ENST00000680137.1:c.8784A>G | ENSP00000505294.1:p.Gln2928= | |
| ENST00000680200.1:c.8784A>G | ENSP00000506166.1:p.Gln2928= | |
| ENST00000680313.1:c.8784A>G | ENSP00000506208.1:p.Gln2928= | |
| ENST00000680423.1:c.*515A>G | ENSP00000505483.1:n.*515A>G | |
| ENST00000680715.1:c.8784A>G | ENSP00000505332.1:p.Gln2928= | |
| ENST00000680808.1:c.8772-197A>G | ENSP00000506446.1:n.8772-197A>G | |
| ENST00000680874.1:c.8784A>G | ENSP00000504911.1:p.Gln2928= | |
| ENST00000681010.1:c.8784A>G | ENSP00000505201.1:p.Gln2928= | |
| ENST00000681066.1:c.8784A>G | ENSP00000506344.1:p.Gln2928= | |
| ENST00000681123.1:c.8784A>G | ENSP00000506124.1:p.Gln2928= | |
| ENST00000681283.1:c.8784A>G | ENSP00000505667.1:p.Gln2928= | |
| ENST00000681311.1:c.*257A>G | ENSP00000505519.1:n.*257A>G | |
| ENST00000681536.1:c.*1983A>G | ENSP00000505821.1:n.*1983A>G | |
| ENST00000681574.1:c.8784A>G | ENSP00000505523.1:p.Gln2928= | |
| ENST00000681822.1:c.8784A>G | ENSP00000505744.1:p.Gln2928= | |
| ENST00000360184.8:c.8784A>G | ENSP00000348965.4:p.Gln2928= | |
| ENST00000555204.1:n.288-197A>G | ||
| NM_001376.4:c.8784A>G | NP_001367.2:p.Gln2928= | |
| NM_001376.5:c.8784A>G MANE Select | NP_001367.2:p.Gln2928= |