Linked Data
ClinVar Variation Id:
137050
dbSNP Id:
rs147641822
ExAC:
11:1780858 G / A
gnomAD v2:
11-1780858-G-A
gnomAD v3:
11-1759628-G-A
gnomAD v4:
11-1759628-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.1759628G>A , CM000673.2:g.1759628G>A | GRCh38 |
| NC_000011.9:g.1780858G>A , CM000673.1:g.1780858G>A | GRCh37 |
| NC_000011.8:g.1737434G>A | NCBI36 |
| NG_008655.1:g.9365C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000236671.7:c.240C>T MANE Select | ENSP00000236671.2:p.Tyr80= | |
| ENST00000367196.4:c.135C>T | ENSP00000356164.4:p.Tyr45= | |
| ENST00000429746.2:c.135C>T | ENSP00000402586.2:p.Tyr45= | |
| ENST00000433655.6:c.240C>T | ENSP00000404902.1:p.Tyr80= | |
| ENST00000438213.6:c.240C>T | ENSP00000415036.2:p.Tyr80= | |
| ENST00000636397.1:c.240C>T | ENSP00000489910.1:p.Tyr80= | |
| ENST00000636571.1:c.219C>T | ENSP00000490770.1:p.Tyr73= | |
| ENST00000636615.1:c.240C>T | ENSP00000490014.1:p.Tyr80= | |
| ENST00000636843.1:c.234C>T | ENSP00000490897.1:p.Tyr78= | |
| ENST00000637381.2:n.2668C>T | ||
| ENST00000637387.1:c.240C>T | ENSP00000490598.1:p.Tyr80= | |
| ENST00000637815.2:c.240C>T | ENSP00000490344.1:p.Tyr80= | |
| ENST00000637915.1:c.240C>T | ENSP00000490471.1:p.Tyr80= | |
| ENST00000677300.1:n.635C>T | ||
| ENST00000678991.1:c.*101C>T | ENSP00000503019.1:n.*101C>T | |
| ENST00000236671.6:c.240C>T | ENSP00000236671.2:p.Tyr80= | |
| ENST00000367196.3:c.135C>T | ENSP00000356164.3:p.Tyr45= | |
| ENST00000433655.5:c.240C>T | ENSP00000404902.1:p.Tyr80= | |
| ENST00000438213.5:c.195C>T | ENSP00000415036.1:p.Tyr65= | |
| NM_001909.4:c.240C>T | NP_001900.1:p.Tyr80= | |
| NM_001909.5:c.240C>T MANE Select | NP_001900.1:p.Tyr80= |