Linked Data
ClinVar Variation Id:
286228
dbSNP Id:
rs778032599
ExAC:
17:78092608 A / G
gnomAD v2:
17-78092608-A-G
gnomAD v3:
17-80118809-A-G
gnomAD v4:
17-80118809-A-G
COSMIC:
COSM5773671
ERepo:
CA8815855/MONDO:0009290/010
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.80118809A>G , CM000679.2:g.80118809A>G | GRCh38 |
| NC_000017.10:g.78092608A>G , CM000679.1:g.78092608A>G | GRCh37 |
| NC_000017.9:g.75707203A>G | NCBI36 |
| NG_009822.1:g.22254A>G , LRG_673:g.22254A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000570803.6:c.2799+4A>G | ENSP00000460543.2:n.2799+4A>G | |
| ENST00000572080.2:c.*937+4A>G | ENSP00000459972.2:n.*937+4A>G | |
| ENST00000577106.6:c.2799+4A>G | ENSP00000458306.2:n.2799+4A>G | |
| ENST00000302262.8:c.2799+4A>G MANE Select | ENSP00000305692.3:n.2799+4A>G | |
| ENST00000302262.7:c.2799+4A>G | ENSP00000305692.3:n.2799+4A>G | |
| ENST00000390015.7:c.2799+4A>G | ENSP00000374665.3:n.2799+4A>G | |
| ENST00000573556.1:n.752+4A>G | ||
| NM_000152.3:c.2799+4A>G , LRG_673t1:c.2799+4A>G | NP_000143.2:n.2799+4A>G | |
| NM_001079803.1:c.2799+4A>G | NP_001073271.1:n.2799+4A>G | |
| NM_001079804.1:c.2799+4A>G | NP_001073272.1:n.2799+4A>G | |
| XM_005257193.1:c.2799+4A>G | XP_005257250.1:n.2799+4A>G | |
| XM_005257194.3:c.2799+4A>G | XP_005257251.1:n.2799+4A>G | |
| NM_000152.4:c.2799+4A>G | NP_000143.2:n.2799+4A>G | |
| NM_001079803.2:c.2799+4A>G | NP_001073271.1:n.2799+4A>G | |
| NM_001079804.2:c.2799+4A>G | NP_001073272.1:n.2799+4A>G | |
| XM_005257193.2:c.2799+4A>G | XP_005257250.1:n.2799+4A>G | |
| XM_005257194.4:c.2799+4A>G | XP_005257251.1:n.2799+4A>G | |
| NM_000152.5:c.2799+4A>G MANE Select | NP_000143.2:n.2799+4A>G | |
| NM_001079803.3:c.2799+4A>G | NP_001073271.1:n.2799+4A>G | |
| NM_001079804.3:c.2799+4A>G | NP_001073272.1:n.2799+4A>G |