Linked Data
ClinVar Variation Id:
96931
dbSNP Id:
rs431825407
ExAC:
17:41234414 T / C
gnomAD v2:
17-41234414-T-C
gnomAD v4:
17-43082397-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43082397T>C , CM000679.2:g.43082397T>C | GRCh38 |
| NC_000017.10:g.41234414T>C , CM000679.1:g.41234414T>C | GRCh37 |
| NC_000017.9:g.38487940T>C | NCBI36 |
| NG_005905.2:g.135587A>G , LRG_292:g.135587A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461574.2:c.4357+7A>G | ENSP00000417241.2:n.4357+7A>G | |
| ENST00000470026.6:c.4357+7A>G | ENSP00000419274.2:n.4357+7A>G | |
| ENST00000473961.6:c.4231+7A>G | ENSP00000420201.2:n.4231+7A>G | |
| ENST00000476777.6:c.4351+7A>G | ENSP00000417554.2:n.4351+7A>G | |
| ENST00000477152.6:c.4279+7A>G | ENSP00000419988.2:n.4279+7A>G | |
| ENST00000478531.6:c.1045+7A>G | ENSP00000420412.2:n.1045+7A>G | |
| ENST00000489037.2:c.4279+7A>G | ENSP00000420781.2:n.4279+7A>G | |
| ENST00000493919.6:c.907+7A>G | ENSP00000418819.2:n.907+7A>G | |
| ENST00000494123.6:c.4357+7A>G | ENSP00000419103.2:n.4357+7A>G | |
| ENST00000497488.2:c.3469+7A>G | ENSP00000418986.2:n.3469+7A>G | |
| ENST00000618469.2:c.4357+7A>G | ENSP00000478114.2:n.4357+7A>G | |
| ENST00000634433.2:c.4234+7A>G | ENSP00000489431.2:n.4234+7A>G | |
| ENST00000644379.2:c.4357+7A>G | ENSP00000496570.2:n.4357+7A>G | |
| ENST00000644555.2:c.907+7A>G | ENSP00000494614.2:n.907+7A>G | |
| ENST00000652672.2:c.4216+7A>G | ENSP00000498906.2:n.4216+7A>G | |
| ENST00000484087.6:c.922+7A>G | ENSP00000419481.2:n.922+7A>G | |
| ENST00000700182.1:c.967+7A>G | ENSP00000514849.1:n.967+7A>G | |
| ENST00000357654.9:c.4357+7A>G MANE Select | ENSP00000350283.3:n.4357+7A>G | |
| ENST00000471181.7:c.4357+7A>G | ENSP00000418960.2:n.4357+7A>G | |
| ENST00000644379.1:c.678+7A>G | ||
| ENST00000352993.7:c.931+7A>G | ENSP00000312236.5:n.931+7A>G | |
| ENST00000357654.7:c.4357+7A>G | ENSP00000350283.3:n.4357+7A>G | |
| ENST00000461221.5:c.*4140+7A>G | ENSP00000418548.1:n.*4140+7A>G | |
| ENST00000461574.1:c.651+7A>G | ||
| ENST00000468300.5:c.1048+7A>G | ENSP00000417148.1:n.1048+7A>G | |
| ENST00000471181.6:c.4357+7A>G | ENSP00000418960.2:n.4357+7A>G | |
| ENST00000478531.5:c.1045+7A>G | ENSP00000420412.1:n.1045+7A>G | |
| ENST00000484087.5:c.670+7A>G | ENSP00000419481.1:n.670+7A>G | |
| ENST00000487825.5:c.673+7A>G | ENSP00000418212.1:n.673+7A>G | |
| ENST00000491747.6:c.1048+7A>G | ENSP00000420705.2:n.1048+7A>G | |
| ENST00000493795.5:c.4216+7A>G | ENSP00000418775.1:n.4216+7A>G | |
| ENST00000493919.5:c.907+7A>G | ENSP00000418819.1:n.907+7A>G | |
| ENST00000586385.5:c.5-18446A>G | ENSP00000465818.1:n.5-18446A>G | |
| ENST00000591534.5:c.-43-7876A>G | ENSP00000467329.1:n.-43-7876A>G | |
| ENST00000591849.5:c.-98-32207A>G | ENSP00000465347.1:n.-98-32207A>G | |
| ENST00000621897.1:n.251+7A>G | ||
| NM_007294.3:c.4357+7A>G , LRG_292t1:c.4357+7A>G | NP_009225.1:n.4357+7A>G | |
| NM_007297.3:c.4216+7A>G | NP_009228.2:n.4216+7A>G | |
| NM_007298.3:c.1048+7A>G | NP_009229.2:n.1048+7A>G | |
| NM_007299.3:c.1048+7A>G | NP_009230.2:n.1048+7A>G | |
| NM_007300.3:c.4357+7A>G | NP_009231.2:n.4357+7A>G | |
| NR_027676.1:n.4493+7A>G | ||
| NM_007294.4:c.4357+7A>G MANE Select | NP_009225.1:n.4357+7A>G | |
| NM_007297.4:c.4216+7A>G | NP_009228.2:n.4216+7A>G | |
| NM_007299.4:c.1048+7A>G | NP_009230.2:n.1048+7A>G | |
| NM_007300.4:c.4357+7A>G | NP_009231.2:n.4357+7A>G | |
| NR_027676.2:n.4534+7A>G |