Linked Data
dbSNP Id:
rs1056233134
gnomAD v3:
9-133454540-C-T
gnomAD v4:
9-133454540-C-T
MyVariant Identifiers:
chr9:g.133454540C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133454540C>T , CM000671.2:g.133454540C>T | GRCh38 |
| NC_000009.10:g.135309483C>T | NCBI36 |
| NG_011934.2:g.45202C>T , LRG_544:g.45202C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355699.7:c.3170C>T MANE Select | ENSP00000347927.2:p.Ala1057Val | |
| ENST00000355699.6:c.3170C>T | ENSP00000347927.2:p.Ala1057Val | |
| ENST00000356589.6:c.3077C>T | ENSP00000348997.2:p.Ala1026Val | |
| ENST00000371916.5:c.*639C>T | ENSP00000360984.2:n.*639C>T | |
| ENST00000371929.7:c.3170C>T | ENSP00000360997.3:p.Ala1057Val | |
| ENST00000485925.5:n.1986C>T | ||
| NM_139025.4:c.3170C>T , LRG_544t1:c.3170C>T | NP_620594.1:p.Ala1057Val | |
| NM_139026.4:c.3077C>T | NP_620595.1:p.Ala1026Val | |
| NM_139027.4:c.3170C>T | NP_620596.2:p.Ala1057Val | |
| NR_024514.2:n.2005C>T | ||
| XM_011518174.1:c.2780C>T | XP_011516476.1:p.Ala927Val | |
| XM_011518175.1:c.3170C>T | XP_011516477.1:p.Ala1057Val | |
| XM_011518176.1:c.2186C>T | XP_011516478.1:p.Ala729Val | |
| XM_011518177.1:c.2180C>T | XP_011516479.1:p.Ala727Val | |
| XM_011518178.1:c.1835C>T | XP_011516480.1:p.Ala612Val | |
| XM_011518179.1:c.1835C>T | XP_011516481.1:p.Ala612Val | |
| XM_011518180.1:c.1436C>T | XP_011516482.1:p.Ala479Val | |
| XM_011518176.3:c.2186C>T | XP_011516478.1:p.Ala729Val | |
| XM_011518178.2:c.1835C>T | XP_011516480.1:p.Ala612Val | |
| XM_017014232.1:c.3158C>T | XP_016869721.1:p.Ala1053Val | |
| XM_017014233.1:c.2780C>T | XP_016869722.1:p.Ala927Val | |
| XM_017014234.2:c.2180C>T | XP_016869723.1:p.Ala727Val | |
| NM_139026.5:c.3077C>T | NP_620595.1:p.Ala1026Val | |
| NM_139027.5:c.3170C>T | NP_620596.2:p.Ala1057Val | |
| NM_139025.5:c.3170C>T | NP_620594.1:p.Ala1057Val | |
| NM_139026.6:c.3077C>T | NP_620595.1:p.Ala1026Val | |
| NM_139027.6:c.3170C>T MANE Select | NP_620596.2:p.Ala1057Val | |
| NR_024514.3:n.2007C>T |