Linked Data
dbSNP Id:
rs898392861
gnomAD v2:
8-117784173-A-G
gnomAD v3:
8-116771934-A-G
gnomAD v4:
8-116771934-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.116771934A>G , CM000670.2:g.116771934A>G | GRCh38 |
| NC_000008.10:g.117784173A>G , CM000670.1:g.117784173A>G | GRCh37 |
| NC_000008.9:g.117853354A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309822.7:c.*92A>G MANE Select | ENSP00000308332.2:n.*92A>G | |
| ENST00000309822.6:c.*92A>G | ENSP00000308332.2:n.*92A>G | |
| ENST00000517814.1:c.363+1568A>G | ENSP00000429962.1:n.363+1568A>G | |
| ENST00000517820.1:c.188+5143A>G | ENSP00000427767.1:n.188+5143A>G | |
| ENST00000520733.5:c.45+1568A>G | ENSP00000429384.1:n.45+1568A>G | |
| ENST00000521071.1:c.188+5143A>G | ENSP00000430029.1:n.188+5143A>G | |
| ENST00000521703.5:c.188+5143A>G | ENSP00000428455.1:n.188+5143A>G | |
| ENST00000524128.1:c.45+1568A>G | ENSP00000430309.1:n.45+1568A>G | |
| NM_032334.2:c.*92A>G | NP_115710.2:n.*92A>G | |
| XM_005251080.2:c.363+1568A>G | XP_005251137.2:n.363+1568A>G | |
| XR_928356.1:n.411+1568A>G | ||
| XR_928357.1:n.411+1568A>G | ||
| NM_032334.3:c.*92A>G MANE Select | NP_115710.2:n.*92A>G |