Linked Data
dbSNP Id:
rs782433445
gnomAD v3:
9-133436895-C-G
gnomAD v4:
9-133436895-C-G
MyVariant Identifiers:
chr9:g.133436895C>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133436895C>G , CM000671.2:g.133436895C>G | GRCh38 |
| NC_000009.10:g.135291836C>G | NCBI36 |
| NG_011934.2:g.27557C>G , LRG_544:g.27557C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355699.7:c.1375C>G MANE Select | ENSP00000347927.2:p.Arg459Gly | |
| ENST00000355699.6:c.1375C>G | ENSP00000347927.2:p.Arg459Gly | |
| ENST00000356589.6:c.1282C>G | ENSP00000348997.2:p.Arg428Gly | |
| ENST00000371916.5:c.631C>G | ENSP00000360984.2:p.Arg211Gly | |
| ENST00000371929.7:c.1375C>G | ENSP00000360997.3:p.Arg459Gly | |
| ENST00000474918.1:c.*179C>G | ENSP00000435305.1:n.*179C>G | |
| ENST00000485925.5:n.974-2471C>G | ||
| ENST00000495234.5:c.*659C>G | ENSP00000435274.1:n.*659C>G | |
| NM_139025.4:c.1375C>G , LRG_544t1:c.1375C>G | NP_620594.1:p.Arg459Gly | |
| NM_139026.4:c.1282C>G | NP_620595.1:p.Arg428Gly | |
| NM_139027.4:c.1375C>G | NP_620596.2:p.Arg459Gly | |
| NR_024514.2:n.993-2471C>G | ||
| XM_011518174.1:c.985C>G | XP_011516476.1:p.Arg329Gly | |
| XM_011518175.1:c.1375C>G | XP_011516477.1:p.Arg459Gly | |
| XM_011518176.1:c.391C>G | XP_011516478.1:p.Arg131Gly | |
| XM_011518177.1:c.385C>G | XP_011516479.1:p.Arg129Gly | |
| XM_011518178.1:c.40C>G | XP_011516480.1:p.Arg14Gly | |
| XM_011518179.1:c.161C>G | XP_011516481.1:p.Ala54Gly | |
| XM_011518180.1:c.687-7968C>G | XP_011516482.1:n.687-7968C>G | |
| XM_011518176.3:c.391C>G | XP_011516478.1:p.Arg131Gly | |
| XM_011518178.2:c.40C>G | XP_011516480.1:p.Arg14Gly | |
| XM_017014232.1:c.1363C>G | XP_016869721.1:p.Arg455Gly | |
| XM_017014233.1:c.985C>G | XP_016869722.1:p.Arg329Gly | |
| XM_017014234.2:c.385C>G | XP_016869723.1:p.Arg129Gly | |
| XM_017014235.1:c.1375C>G | XP_016869724.1:p.Arg459Gly | |
| XR_001746171.1:n.2600C>G | ||
| NM_139026.5:c.1282C>G | NP_620595.1:p.Arg428Gly | |
| NM_139027.5:c.1375C>G | NP_620596.2:p.Arg459Gly | |
| NM_139025.5:c.1375C>G | NP_620594.1:p.Arg459Gly | |
| NM_139026.6:c.1282C>G | NP_620595.1:p.Arg428Gly | |
| NM_139027.6:c.1375C>G MANE Select | NP_620596.2:p.Arg459Gly | |
| NR_024514.3:n.995-2471C>G |