Linked Data
ClinVar Variation Id:
286107
dbSNP Id:
rs886043311
gnomAD v3:
1-197438685-A-G
gnomAD v4:
1-197438685-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.197438685A>G , CM000663.2:g.197438685A>G | GRCh38 |
| NC_000001.10:g.197407815A>G , CM000663.1:g.197407815A>G | GRCh37 |
| NC_000001.9:g.195674438A>G | NCBI36 |
| NG_008483.1:g.175408A>G | |
| NG_008483.2:g.242224A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367400.8:c.3878+10A>G MANE Select | ENSP00000356370.3:n.3878+10A>G | |
| ENST00000638467.1:c.3878+10A>G | ENSP00000491102.1:n.3878+10A>G | |
| ENST00000681519.1:c.2759+10A>G | ENSP00000505267.1:n.2759+10A>G | |
| ENST00000367397.1:c.*6A>G | ENSP00000356367.1:n.*6A>G | |
| ENST00000367399.6:c.3542+10A>G | ENSP00000356369.2:n.3542+10A>G | |
| ENST00000367400.7:c.3878+10A>G | ENSP00000356370.3:n.3878+10A>G | |
| ENST00000484075.5:c.3878+10A>G | ENSP00000433932.1:n.3878+10A>G | |
| ENST00000535699.5:c.3806+10A>G | ENSP00000438786.1:n.3806+10A>G | |
| ENST00000538660.5:c.2270+10A>G | ENSP00000438091.1:n.2270+10A>G | |
| NM_001193640.1:c.3542+10A>G | NP_001180569.1:n.3542+10A>G | |
| NM_001257965.1:c.3806+10A>G | NP_001244894.1:n.3806+10A>G | |
| NM_001257966.1:c.2270+10A>G | NP_001244895.1:n.2270+10A>G | |
| NM_201253.2:c.3878+10A>G | NP_957705.1:n.3878+10A>G | |
| NR_047563.1:n.3879+10A>G | ||
| NR_047564.1:n.4087+10A>G | ||
| XM_011509365.1:c.3878+10A>G | XP_011507667.1:n.3878+10A>G | |
| XM_011509366.1:c.3878+10A>G | XP_011507668.1:n.3878+10A>G | |
| XM_011509367.1:c.3878+10A>G | XP_011507669.1:n.3878+10A>G | |
| XM_011509368.1:c.3296+10A>G | XP_011507670.1:n.3296+10A>G | |
| XM_011509369.1:c.2321+10A>G | XP_011507671.1:n.2321+10A>G | |
| XM_011509365.2:c.3878+10A>G | XP_011507667.1:n.3878+10A>G | |
| XM_011509369.2:c.2321+10A>G | XP_011507671.1:n.2321+10A>G | |
| XM_017000851.1:c.3035+10A>G | XP_016856340.1:n.3035+10A>G | |
| XM_017000852.1:c.4013+10A>G | XP_016856341.1:n.4013+10A>G | |
| NM_201253.3:c.3878+10A>G MANE Select | NP_957705.1:n.3878+10A>G | |
| NM_001193640.2:c.3542+10A>G | NP_001180569.1:n.3542+10A>G | |
| NM_001257965.2:c.3806+10A>G | NP_001244894.1:n.3806+10A>G | |
| NR_047563.2:n.3831+10A>G | ||
| NR_047564.2:n.4039+10A>G | ||
| NM_001257966.2:c.2270+10A>G | NP_001244895.1:n.2270+10A>G |