Linked Data
ClinVar Variation Id:
128923
dbSNP Id:
rs377669980
ExAC:
14:102508077 G / A
gnomAD v2:
14-102508077-G-A
gnomAD v3:
14-102041740-G-A
gnomAD v4:
14-102041740-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.102041740G>A , CM000676.2:g.102041740G>A | GRCh38 |
| NC_000014.8:g.102508077G>A , CM000676.1:g.102508077G>A | GRCh37 |
| NC_000014.7:g.101577830G>A | NCBI36 |
| NG_008777.1:g.82213G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684561.1:c.*3561+6G>A | ENSP00000506816.1:n.*3561+6G>A | |
| ENST00000360184.10:c.12102+6G>A MANE Select | ENSP00000348965.4:n.12102+6G>A | |
| ENST00000553701.1:n.347-4971C>T | ||
| ENST00000556139.2:n.654+6G>A | ||
| ENST00000556499.3:n.1235+6G>A | ||
| ENST00000557242.1:n.329-4971C>T | ||
| ENST00000557551.1:n.111+2553C>T | ||
| ENST00000643437.1:n.2056+6G>A | ||
| ENST00000643829.1:n.1931+6G>A | ||
| ENST00000644794.1:n.2221+6G>A | ||
| ENST00000644881.2:c.12102+6G>A | ENSP00000495022.2:n.12102+6G>A | |
| ENST00000644888.1:n.81G>A | ||
| ENST00000645039.2:c.11851+6G>A | ENSP00000495220.2:n.11851+6G>A | |
| ENST00000645085.1:n.348+6G>A | ||
| ENST00000645149.2:c.11955+6G>A | ENSP00000495944.2:n.11955+6G>A | |
| ENST00000645697.1:n.2765+6G>A | ||
| ENST00000647204.2:n.1343+6G>A | ||
| ENST00000647366.1:n.5656+6G>A | ||
| ENST00000679486.1:c.12102+6G>A | ENSP00000506688.1:n.12102+6G>A | |
| ENST00000679629.1:c.*125+6G>A | ENSP00000505589.1:n.*125+6G>A | |
| ENST00000679720.1:c.12102+6G>A | ENSP00000505938.1:n.12102+6G>A | |
| ENST00000679910.1:c.*3184+6G>A | ENSP00000506521.1:n.*3184+6G>A | |
| ENST00000680120.1:c.12102+6G>A | ENSP00000504863.1:n.12102+6G>A | |
| ENST00000680200.1:c.*1361+6G>A | ENSP00000506166.1:n.*1361+6G>A | |
| ENST00000680313.1:c.12102+6G>A | ENSP00000506208.1:n.12102+6G>A | |
| ENST00000680423.1:c.*3833+6G>A | ENSP00000505483.1:n.*3833+6G>A | |
| ENST00000680715.1:c.12102+6G>A | ENSP00000505332.1:n.12102+6G>A | |
| ENST00000681010.1:c.12102+6G>A | ENSP00000505201.1:n.12102+6G>A | |
| ENST00000681066.1:c.*125+6G>A | ENSP00000506344.1:n.*125+6G>A | |
| ENST00000681123.1:c.*125+6G>A | ENSP00000506124.1:n.*125+6G>A | |
| ENST00000681283.1:c.*814+6G>A | ENSP00000505667.1:n.*814+6G>A | |
| ENST00000681536.1:c.*5301+6G>A | ENSP00000505821.1:n.*5301+6G>A | |
| ENST00000681574.1:c.12102+6G>A | ENSP00000505523.1:n.12102+6G>A | |
| ENST00000681822.1:c.12102+6G>A | ENSP00000505744.1:n.12102+6G>A | |
| ENST00000360184.8:c.12102+6G>A | ENSP00000348965.4:n.12102+6G>A | |
| ENST00000556139.1:n.654+6G>A | ||
| NM_001376.4:c.12102+6G>A | NP_001367.2:n.12102+6G>A | |
| NM_001376.5:c.12102+6G>A MANE Select | NP_001367.2:n.12102+6G>A |