Linked Data
dbSNP Id:
rs746976470
ExAC:
2:238267932 T / C
gnomAD v2:
2-238267932-T-C
gnomAD v4:
2-237359289-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.237359289T>C , CM000664.2:g.237359289T>C | GRCh38 |
| NC_000002.11:g.238267932T>C , CM000664.1:g.238267932T>C | GRCh37 |
| NC_000002.10:g.237932671T>C | NCBI36 |
| NG_008676.1:g.59919A>G , LRG_473:g.59919A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000353578.9:c.5692-39A>G | ENSP00000315873.4:n.5692-39A>G | |
| ENST00000295550.9:c.6310-39A>G MANE Select | ENSP00000295550.4:n.6310-39A>G | |
| ENST00000295550.8:c.6310-39A>G | ENSP00000295550.4:n.6310-39A>G | |
| ENST00000347401.7:c.4489-39A>G | ENSP00000315609.4:n.4489-39A>G | |
| ENST00000353578.8:c.5692-39A>G | ENSP00000315873.4:n.5692-39A>G | |
| ENST00000409809.5:c.5692-39A>G | ENSP00000386844.1:n.5692-39A>G | |
| ENST00000472056.5:c.4489-39A>G | ENSP00000418285.1:n.4489-39A>G | |
| NM_004369.3:c.6310-39A>G , LRG_473t1:c.6310-39A>G | NP_004360.2:n.6310-39A>G | |
| NM_057166.4:c.4489-39A>G | NP_476507.3:n.4489-39A>G | |
| NM_057167.3:c.5692-39A>G | NP_476508.2:n.5692-39A>G | |
| XM_005246065.1:c.5710-39A>G | XP_005246122.1:n.5710-39A>G | |
| XM_005246066.1:c.5089-39A>G | XP_005246123.1:n.5089-39A>G | |
| XM_006712253.1:c.5809-39A>G | XP_006712316.1:n.5809-39A>G | |
| XM_011510574.1:c.6307-39A>G | XP_011508876.1:n.6307-39A>G | |
| XM_011510575.1:c.3904-39A>G | XP_011508877.1:n.3904-39A>G | |
| XM_017003304.1:c.3904-39A>G | XP_016858793.1:n.3904-39A>G | |
| XM_024452684.1:c.5089-39A>G | XP_024308452.1:n.5089-39A>G | |
| NM_004369.4:c.6310-39A>G MANE Select | NP_004360.2:n.6310-39A>G | |
| NM_057166.5:c.4489-39A>G | NP_476507.3:n.4489-39A>G | |
| NM_057167.4:c.5692-39A>G | NP_476508.2:n.5692-39A>G |