Linked Data
dbSNP Id:
rs1418762410
gnomAD v2:
8-117783780-C-G
gnomAD v3:
8-116771541-C-G
gnomAD v4:
8-116771541-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.116771541C>G , CM000670.2:g.116771541C>G | GRCh38 |
| NC_000008.10:g.117783780C>G , CM000670.1:g.117783780C>G | GRCh37 |
| NC_000008.9:g.117852961C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309822.7:c.449C>G MANE Select | ENSP00000308332.2:p.Pro150Arg | |
| ENST00000309822.6:c.449C>G | ENSP00000308332.2:p.Pro150Arg | |
| ENST00000517814.1:c.363+1175C>G | ENSP00000429962.1:n.363+1175C>G | |
| ENST00000517820.1:c.188+4750C>G | ENSP00000427767.1:n.188+4750C>G | |
| ENST00000520733.5:c.45+1175C>G | ENSP00000429384.1:n.45+1175C>G | |
| ENST00000521071.1:c.188+4750C>G | ENSP00000430029.1:n.188+4750C>G | |
| ENST00000521703.5:c.188+4750C>G | ENSP00000428455.1:n.188+4750C>G | |
| ENST00000521974.1:n.355C>G | ||
| ENST00000524128.1:c.45+1175C>G | ENSP00000430309.1:n.45+1175C>G | |
| NM_032334.2:c.449C>G | NP_115710.2:p.Pro150Arg | |
| XM_005251080.2:c.363+1175C>G | XP_005251137.2:n.363+1175C>G | |
| XR_928356.1:n.411+1175C>G | ||
| XR_928357.1:n.411+1175C>G | ||
| NM_032334.3:c.449C>G MANE Select | NP_115710.2:p.Pro150Arg |