Linked Data
dbSNP Id:
rs778573585
gnomAD v2:
11-45827925-A-G
gnomAD v3:
11-45806374-A-G
gnomAD v4:
11-45806374-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.45806374A>G , CM000673.2:g.45806374A>G | GRCh38 |
| NC_000011.9:g.45827925A>G , CM000673.1:g.45827925A>G | GRCh37 |
| NC_000011.8:g.45784501A>G | NCBI36 |
| NG_009875.1:g.7303A>G , LRG_107:g.7303A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000526817.2:c.496+38A>G | ENSP00000432145.2:n.496+38A>G | |
| ENST00000314134.4:c.535+38A>G MANE Select | ENSP00000313318.3:n.535+38A>G | |
| ENST00000314134.3:c.535+38A>G | ENSP00000313318.3:n.535+38A>G | |
| ENST00000442528.2:c.496+38A>G | ENSP00000412408.2:n.496+38A>G | |
| NM_001145265.1:c.496+38A>G | NP_001138737.1:n.496+38A>G | |
| NM_001145266.1:c.496+38A>G | NP_001138738.1:n.496+38A>G | |
| NM_018389.4:c.535+38A>G , LRG_107t1:c.535+38A>G | NP_060859.4:n.535+38A>G | |
| XM_011520203.1:c.535+38A>G | XP_011518505.1:n.535+38A>G | |
| XM_011520203.3:c.535+38A>G | XP_011518505.1:n.535+38A>G | |
| NM_001145265.2:c.496+38A>G | NP_001138737.1:n.496+38A>G | |
| NM_018389.5:c.535+38A>G MANE Select | NP_060859.4:n.535+38A>G |