Linked Data
ClinVar Variation Id:
382875
dbSNP Id:
rs756924858
ExAC:
14:102493050 C / A
gnomAD v2:
14-102493050-C-A
gnomAD v4:
14-102026713-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.102026713C>A , CM000676.2:g.102026713C>A | GRCh38 |
| NC_000014.8:g.102493050C>A , CM000676.1:g.102493050C>A | GRCh37 |
| NC_000014.7:g.101562803C>A | NCBI36 |
| NG_008777.1:g.67186C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684561.1:c.*230+6C>A | ENSP00000506816.1:n.*230+6C>A | |
| ENST00000360184.10:c.8771+6C>A MANE Select | ENSP00000348965.4:n.8771+6C>A | |
| ENST00000643508.2:c.8771+6C>A | ENSP00000495528.2:n.8771+6C>A | |
| ENST00000644881.2:c.8771+6C>A | ENSP00000495022.2:n.8771+6C>A | |
| ENST00000645039.2:c.8771+6C>A | ENSP00000495220.2:n.8771+6C>A | |
| ENST00000645149.2:c.8771+6C>A | ENSP00000495944.2:n.8771+6C>A | |
| ENST00000647366.1:n.2325+6C>A | ||
| ENST00000679486.1:c.8771+6C>A | ENSP00000506688.1:n.8771+6C>A | |
| ENST00000679629.1:c.8771+6C>A | ENSP00000505589.1:n.8771+6C>A | |
| ENST00000679720.1:c.8771+6C>A | ENSP00000505938.1:n.8771+6C>A | |
| ENST00000679910.1:c.8771+6C>A | ENSP00000506521.1:n.8771+6C>A | |
| ENST00000680120.1:c.8771+6C>A | ENSP00000504863.1:n.8771+6C>A | |
| ENST00000680137.1:c.8771+6C>A | ENSP00000505294.1:n.8771+6C>A | |
| ENST00000680200.1:c.8771+6C>A | ENSP00000506166.1:n.8771+6C>A | |
| ENST00000680313.1:c.8771+6C>A | ENSP00000506208.1:n.8771+6C>A | |
| ENST00000680423.1:c.*502+6C>A | ENSP00000505483.1:n.*502+6C>A | |
| ENST00000680715.1:c.8771+6C>A | ENSP00000505332.1:n.8771+6C>A | |
| ENST00000680808.1:c.8771+6C>A | ENSP00000506446.1:n.8771+6C>A | |
| ENST00000680874.1:c.8771+6C>A | ENSP00000504911.1:n.8771+6C>A | |
| ENST00000681010.1:c.8771+6C>A | ENSP00000505201.1:n.8771+6C>A | |
| ENST00000681066.1:c.8771+6C>A | ENSP00000506344.1:n.8771+6C>A | |
| ENST00000681123.1:c.8771+6C>A | ENSP00000506124.1:n.8771+6C>A | |
| ENST00000681283.1:c.8771+6C>A | ENSP00000505667.1:n.8771+6C>A | |
| ENST00000681311.1:c.*244+6C>A | ENSP00000505519.1:n.*244+6C>A | |
| ENST00000681536.1:c.*1970+6C>A | ENSP00000505821.1:n.*1970+6C>A | |
| ENST00000681574.1:c.8771+6C>A | ENSP00000505523.1:n.8771+6C>A | |
| ENST00000681822.1:c.8771+6C>A | ENSP00000505744.1:n.8771+6C>A | |
| ENST00000360184.8:c.8771+6C>A | ENSP00000348965.4:n.8771+6C>A | |
| ENST00000555204.1:n.287+6C>A | ||
| NM_001376.4:c.8771+6C>A | NP_001367.2:n.8771+6C>A | |
| NM_001376.5:c.8771+6C>A MANE Select | NP_001367.2:n.8771+6C>A |