Linked Data
ClinVar Variation Id:
306550
ClinVar RCV Id:
RCV000370567
dbSNP Id:
rs376521838
gnomAD v3:
11-9778732-C-T
gnomAD v4:
11-9778732-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.9778732C>T , CM000673.2:g.9778732C>T | GRCh38 |
| NC_000011.9:g.9800279C>T , CM000673.1:g.9800279C>T | GRCh37 |
| NC_000011.8:g.9756855C>T | NCBI36 |
| NG_008074.1:g.520476G>A , LRG_267:g.520476G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000689940.1:c.*1686G>A (SBF2) | ENSP00000508452.1:n.*1686G>A | |
| ENST00000690944.1:c.3316G>A (SBF2) | ||
| ENST00000692716.1:c.*1686G>A (SBF2) | ENSP00000509545.1:n.*1686G>A | |
| ENST00000256190.13:c.*1686G>A (SBF2) MANE Select | ENSP00000256190.8:n.*1686G>A | |
| ENST00000676324.1:c.*3544G>A (SBF2) | ENSP00000502578.1:n.*3544G>A | |
| ENST00000256190.12:c.*1686G>A (SBF2) | ENSP00000256190.8:n.*1686G>A | |
| ENST00000617179.4:c.7095G>A (SBF2) | ENSP00000482806.1:n.7095G>A | |
| NM_030962.3:c.*1686G>A , LRG_267t1:c.*1686G>A (SBF2) | NP_112224.1:n.*1686G>A | |
| NR_036485.1:n.211+20229C>T (SBF2-AS1) | ||
| XM_005253154.3:c.*1686G>A (SBF2) | XP_005253211.1:n.*1686G>A | |
| XM_005253155.3:c.*1686G>A (SBF2) | XP_005253212.1:n.*1686G>A | |
| XM_011520394.1:c.*1686G>A (SBF2) | XP_011518696.1:n.*1686G>A | |
| XM_005253154.5:c.*1686G>A (SBF2) | XP_005253211.1:n.*1686G>A | |
| XM_005253155.5:c.*1686G>A (SBF2) | XP_005253212.1:n.*1686G>A | |
| XM_011520394.3:c.*1686G>A (SBF2) | XP_011518696.1:n.*1686G>A | |
| XM_017018372.2:c.*1686G>A (SBF2) | XP_016873861.1:n.*1686G>A | |
| XM_017018373.2:c.*1686G>A (SBF2) | XP_016873862.1:n.*1686G>A | |
| XM_017018374.2:c.*1686G>A (SBF2) | XP_016873863.1:n.*1686G>A | |
| XM_017018375.2:c.*1686G>A (SBF2) | XP_016873864.1:n.*1686G>A | |
| NM_001386339.1:c.*1686G>A (SBF2) | NP_001373268.1:n.*1686G>A | |
| NM_001386342.1:c.*1686G>A (SBF2) | NP_001373271.1:n.*1686G>A | |
| NM_030962.4:c.*1686G>A (SBF2) MANE Select | NP_112224.1:n.*1686G>A |