Linked Data
ClinVar Variation Id:
234378
dbSNP Id:
rs145732290
ExAC:
12:110013954 A / G
gnomAD v2:
12-110013954-A-G
gnomAD v3:
12-109576149-A-G
gnomAD v4:
12-109576149-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.109576149A>G , CM000674.2:g.109576149A>G | GRCh38 |
| NC_000012.11:g.110013954A>G , CM000674.1:g.110013954A>G | GRCh37 |
| NC_000012.10:g.108498337A>G | NCBI36 |
| NG_007096.1:g.2349T>C | |
| NG_007702.1:g.7455A>G , LRG_156:g.7455A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000539696.6:c.-92+2276A>G | ENSP00000439134.1:n.-92+2276A>G | |
| ENST00000546277.6:c.226+4A>G | ENSP00000438153.2:n.226+4A>G | |
| ENST00000636529.2:n.78+1249A>G | ||
| ENST00000697195.1:c.226+4A>G | ENSP00000513181.1:n.226+4A>G | |
| ENST00000697196.1:c.226+4A>G | ENSP00000513182.1:n.226+4A>G | |
| ENST00000228510.8:c.226+4A>G MANE Select | ENSP00000228510.3:n.226+4A>G | |
| ENST00000636529.1:c.64+1249A>G | ||
| ENST00000636996.1:c.219+4A>G | ||
| ENST00000639206.1:c.226+4A>G | ENSP00000492778.1:n.226+4A>G | |
| ENST00000228510.7:c.226+4A>G | ENSP00000228510.3:n.226+4A>G | |
| ENST00000392727.7:c.226+4A>G | ENSP00000376487.3:n.226+4A>G | |
| ENST00000447878.6:c.226+4A>G | ENSP00000415555.2:n.226+4A>G | |
| ENST00000535044.1:n.471+4A>G | ||
| ENST00000537237.5:c.226+4A>G | ENSP00000445382.1:n.226+4A>G | |
| ENST00000539335.5:c.226+4A>G | ENSP00000440379.1:n.226+4A>G | |
| ENST00000539575.4:c.226+4A>G | ENSP00000443551.2:n.226+4A>G | |
| ENST00000539696.5:c.-92+2276A>G | ENSP00000439134.1:n.-92+2276A>G | |
| ENST00000545774.5:c.226+4A>G | ENSP00000443978.1:n.226+4A>G | |
| ENST00000546277.5:c.226+4A>G | ENSP00000438153.1:n.226+4A>G | |
| ENST00000625889.2:c.226+4A>G | ENSP00000486846.1:n.226+4A>G | |
| ENST00000629016.2:c.226+4A>G | ENSP00000486804.1:n.226+4A>G | |
| NM_000431.3:c.226+4A>G | NP_000422.1:n.226+4A>G | |
| NM_001114185.2:c.226+4A>G | NP_001107657.1:n.226+4A>G | |
| NM_001301182.1:c.226+4A>G | NP_001288111.1:n.226+4A>G | |
| XM_011538372.1:c.226+4A>G | XP_011536674.1:n.226+4A>G | |
| XM_017019313.2:c.226+4A>G | XP_016874802.1:n.226+4A>G | |
| XM_017019314.1:c.226+4A>G | XP_016874803.1:n.226+4A>G | |
| XM_024448982.1:c.226+4A>G | XP_024304750.1:n.226+4A>G | |
| NM_000431.4:c.226+4A>G MANE Select | NP_000422.1:n.226+4A>G | |
| NM_001114185.3:c.226+4A>G | NP_001107657.1:n.226+4A>G | |
| NM_001301182.2:c.226+4A>G | NP_001288111.1:n.226+4A>G |