Linked Data
ClinVar Variation Id:
1141855
ClinVar RCV Id:
RCV001479417
dbSNP Id:
rs1829567186
gnomAD v4:
9-35094253-T-C
MyVariant Identifiers:
chr9:g.35094250T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.35094253T>C , CM000671.2:g.35094253T>C | GRCh38 |
| NC_000009.11:g.35094250T>C , CM000671.1:g.35094250T>C | GRCh37 |
| NC_000009.10:g.35084250T>C | NCBI36 |
| NG_031990.1:g.7349A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361778.7:c.618A>G | ENSP00000354678.2:p.Thr206= | |
| ENST00000700254.1:c.618A>G | ENSP00000514892.1:p.Thr206= | |
| ENST00000700255.1:c.618A>G | ENSP00000514893.1:p.Thr206= | |
| ENST00000700256.1:n.650A>G | ||
| ENST00000700257.1:c.618A>G | ENSP00000514894.1:p.Thr206= | |
| ENST00000700259.1:c.618A>G | ENSP00000514895.1:p.Thr206= | |
| ENST00000700260.1:c.618A>G | ENSP00000514896.1:p.Thr206= | |
| ENST00000700261.1:c.618A>G | ENSP00000514897.1:p.Thr206= | |
| ENST00000700262.1:c.618A>G | ENSP00000514898.1:p.Thr206= | |
| ENST00000700263.1:c.618A>G | ENSP00000514899.1:p.Thr206= | |
| ENST00000700264.1:c.618A>G | ENSP00000514900.1:p.Thr206= | |
| ENST00000378617.4:c.618A>G MANE Select | ENSP00000367880.3:p.Thr206= | |
| ENST00000298004.9:c.618A>G | ENSP00000298004.5:p.Thr206= | |
| ENST00000361778.6:c.618A>G | ENSP00000354678.2:p.Thr206= | |
| ENST00000378617.3:c.618A>G | ENSP00000367880.3:p.Thr206= | |
| ENST00000465745.6:n.635A>G | ||
| ENST00000472208.1:n.719A>G | ||
| ENST00000474436.1:n.1603A>G | ||
| NM_001201484.1:c.618A>G | NP_001188413.1:p.Thr206= | |
| NM_032634.3:c.618A>G | NP_116023.2:p.Thr206= | |
| NM_152850.3:c.618A>G | NP_690577.2:p.Thr206= | |
| XM_005251619.2:c.618A>G | XP_005251676.1:p.Thr206= | |
| XM_011518056.1:c.618A>G | XP_011516358.1:p.Thr206= | |
| XR_242515.1:n.639A>G | ||
| XM_005251619.3:c.618A>G | XP_005251676.1:p.Thr206= | |
| XM_017015222.2:c.618A>G | XP_016870711.1:p.Thr206= | |
| XM_017015223.1:c.618A>G | XP_016870712.1:p.Thr206= | |
| XM_017015224.1:c.618A>G | XP_016870713.1:p.Thr206= | |
| XR_001746390.1:n.1041A>G | ||
| XR_001746391.2:n.639A>G | ||
| XR_242515.3:n.639A>G | ||
| NM_032634.4:c.618A>G MANE Select | NP_116023.2:p.Thr206= | |
| NM_001201484.2:c.618A>G | NP_001188413.1:p.Thr206= | |
| NM_152850.4:c.618A>G | NP_690577.2:p.Thr206= |