Linked Data
ClinVar Variation Id:
297966
dbSNP Id:
rs766753209
ExAC:
1:6533298 T / C
gnomAD v2:
1-6533298-T-C
gnomAD v3:
1-6473238-T-C
gnomAD v4:
1-6473238-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.6473238T>C , CM000663.2:g.6473238T>C | GRCh38 |
| NC_000001.10:g.6533298T>C , CM000663.1:g.6533298T>C | GRCh37 |
| NC_000001.9:g.6455885T>C | NCBI36 |
| NG_007978.1:g.51772A>G , LRG_262:g.51772A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000340850.10:c.795+13A>G | ENSP00000344570.5:n.795+13A>G | |
| ENST00000377728.8:c.795+13A>G MANE Select | ENSP00000366957.3:n.795+13A>G | |
| ENST00000377740.5:c.795+13A>G | ENSP00000366969.4:n.795+13A>G | |
| ENST00000377748.6:c.969+13A>G | ENSP00000366977.2:n.969+13A>G | |
| ENST00000400913.6:c.795+13A>G | ENSP00000383704.1:n.795+13A>G | |
| ENST00000400915.8:c.906+13A>G | ENSP00000383706.4:n.906+13A>G | |
| ENST00000489097.6:n.1271+13A>G | ||
| ENST00000535355.6:c.1002+13A>G | ENSP00000441445.1:n.1002+13A>G | |
| ENST00000537245.6:c.906+13A>G | ENSP00000439625.2:n.906+13A>G | |
| ENST00000673471.2:c.1092+13A>G | ENSP00000500749.1:n.1092+13A>G | |
| ENST00000674790.1:c.*1007+13A>G | ENSP00000502815.1:n.*1007+13A>G | |
| ENST00000675123.1:c.795+13A>G | ENSP00000502132.1:n.795+13A>G | |
| ENST00000675548.1:c.*623+13A>G | ENSP00000502684.1:n.*623+13A>G | |
| ENST00000675694.1:c.795+13A>G | ENSP00000501925.1:n.795+13A>G | |
| ENST00000340850.9:c.795+13A>G | ENSP00000344570.5:n.795+13A>G | |
| ENST00000377725.5:c.795+13A>G | ENSP00000366954.1:n.795+13A>G | |
| ENST00000377728.7:c.795+13A>G | ENSP00000366957.3:n.795+13A>G | |
| ENST00000377732.5:c.906+13A>G | ENSP00000366961.1:n.906+13A>G | |
| ENST00000377740.4:c.1026+13A>G | ENSP00000366969.3:n.1026+13A>G | |
| ENST00000377748.5:c.1026+13A>G | ENSP00000366977.1:n.1026+13A>G | |
| ENST00000400913.5:c.795+13A>G | ENSP00000383704.1:n.795+13A>G | |
| ENST00000400915.7:c.963+13A>G | ENSP00000383706.3:n.963+13A>G | |
| ENST00000489097.5:n.1271+13A>G | ||
| ENST00000535355.5:c.1002+13A>G | ENSP00000441445.1:n.1002+13A>G | |
| ENST00000537245.5:c.1032+13A>G | ENSP00000439625.1:n.1032+13A>G | |
| NM_001042663.1:c.963+13A>G | NP_001036128.1:n.963+13A>G | |
| NM_001042664.1:c.795+13A>G | NP_001036129.1:n.795+13A>G | |
| NM_001042665.1:c.795+13A>G | NP_001036130.1:n.795+13A>G | |
| NM_001265592.1:c.1032+13A>G | NP_001252521.1:n.1032+13A>G | |
| NM_001265593.1:c.1002+13A>G | NP_001252522.1:n.1002+13A>G | |
| NM_001265594.1:c.795+13A>G | NP_001252523.1:n.795+13A>G | |
| NM_020631.4:c.795+13A>G | NP_065682.2:n.795+13A>G | |
| NM_198681.3:c.1026+13A>G | NP_941374.2:n.1026+13A>G | |
| NM_001042663.2:c.963+13A>G | NP_001036128.1:n.963+13A>G | |
| NM_001265594.2:c.795+13A>G | NP_001252523.1:n.795+13A>G | |
| NM_020631.5:c.795+13A>G | NP_065682.2:n.795+13A>G | |
| NM_001042663.3:c.906+13A>G | NP_001036128.2:n.906+13A>G | |
| NM_001265592.2:c.906+13A>G | NP_001252521.2:n.906+13A>G | |
| NM_020631.6:c.795+13A>G MANE Select | NP_065682.2:n.795+13A>G | |
| NM_198681.4:c.795+13A>G | NP_941374.3:n.795+13A>G |