Linked Data
ClinVar Variation Id:
2055804
ClinVar RCV Id:
RCV002938229
dbSNP Id:
rs2093206049
gnomAD v3:
15-68211749-G-A
gnomAD v4:
15-68211749-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.68211749G>A , CM000677.2:g.68211749G>A | GRCh38 |
| NC_000015.9:g.68504087G>A , CM000677.1:g.68504087G>A | GRCh37 |
| NC_000015.8:g.66291141G>A | NCBI36 |
| NG_008764.2:g.50463C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000249806.11:c.412C>T MANE Select | ENSP00000249806.5:p.Leu138Phe | |
| ENST00000562767.2:c.84-14121C>T | ENSP00000456336.1:n.84-14121C>T | |
| ENST00000563917.2:n.254C>T | ||
| ENST00000565471.6:c.84-1990C>T | ENSP00000457384.1:n.84-1990C>T | |
| ENST00000635747.1:c.*315C>T | ENSP00000490627.1:n.*315C>T | |
| ENST00000636212.1:c.298-8C>T | ENSP00000489851.1:n.298-8C>T | |
| ENST00000636314.1:c.183-431C>T | ENSP00000490295.1:n.183-431C>T | |
| ENST00000636674.1:n.1395C>T | ||
| ENST00000636964.1:n.1584C>T | ||
| ENST00000637054.1:c.198+6787C>T | ENSP00000490807.1:n.198+6787C>T | |
| ENST00000637223.1:c.*201-431C>T | ENSP00000490010.1:n.*201-431C>T | |
| ENST00000637329.1:c.381C>T | ||
| ENST00000637450.1:c.*66C>T | ENSP00000490204.1:n.*66C>T | |
| ENST00000637494.1:c.199-431C>T | ENSP00000490057.1:n.199-431C>T | |
| ENST00000637667.1:c.313C>T | ENSP00000489843.1:p.Leu105Phe | |
| ENST00000637823.1:c.224-106C>T | ||
| ENST00000637888.1:c.198+6787C>T | ENSP00000490546.1:n.198+6787C>T | |
| ENST00000638076.1:c.412C>T | ENSP00000490373.1:p.Leu138Phe | |
| ENST00000638144.1:n.130-431C>T | ||
| ENST00000646164.1:c.38+6787C>T | ||
| ENST00000249806.9:c.412C>T | ENSP00000249806.5:p.Leu138Phe | |
| ENST00000538696.5:c.508C>T | ENSP00000445770.1:p.Leu170Phe | |
| ENST00000562767.1:c.84-14121C>T | ENSP00000456336.1:n.84-14121C>T | |
| ENST00000563917.1:n.193C>T | ||
| ENST00000564752.1:c.412C>T | ENSP00000457822.1:p.Leu138Phe | |
| ENST00000565471.5:c.84-1990C>T | ENSP00000457384.1:n.84-1990C>T | |
| ENST00000566347.5:c.298-431C>T | ENSP00000457783.1:n.298-431C>T | |
| ENST00000567060.5:c.298-2029C>T | ENSP00000454818.1:n.298-2029C>T | |
| NM_017882.2:c.412C>T | NP_060352.1:p.Leu138Phe | |
| XR_931861.1:n.515C>T | ||
| NM_017882.3:c.412C>T MANE Select | NP_060352.1:p.Leu138Phe |