Linked Data
ClinVar Variation Id:
1015733
dbSNP Id:
rs781133812
ExAC:
15:68504182 C / T
gnomAD v2:
15-68504182-C-T
gnomAD v3:
15-68211844-C-T
gnomAD v4:
15-68211844-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.68211844C>T , CM000677.2:g.68211844C>T | GRCh38 |
| NC_000015.9:g.68504182C>T , CM000677.1:g.68504182C>T | GRCh37 |
| NC_000015.8:g.66291236C>T | NCBI36 |
| NG_008764.2:g.50368G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000249806.11:c.317G>A MANE Select | ENSP00000249806.5:p.Arg106His | |
| ENST00000562767.2:c.84-14216G>A | ENSP00000456336.1:n.84-14216G>A | |
| ENST00000563917.2:n.159G>A | ||
| ENST00000565471.6:c.84-2085G>A | ENSP00000457384.1:n.84-2085G>A | |
| ENST00000635747.1:c.*220G>A | ENSP00000490627.1:n.*220G>A | |
| ENST00000636212.1:c.298-103G>A | ENSP00000489851.1:n.298-103G>A | |
| ENST00000636314.1:c.183-526G>A | ENSP00000490295.1:n.183-526G>A | |
| ENST00000636674.1:n.1300G>A | ||
| ENST00000636964.1:n.1489G>A | ||
| ENST00000637054.1:c.198+6692G>A | ENSP00000490807.1:n.198+6692G>A | |
| ENST00000637223.1:c.*201-526G>A | ENSP00000490010.1:n.*201-526G>A | |
| ENST00000637329.1:c.286G>A | ||
| ENST00000637450.1:c.202G>A | ENSP00000490204.1:p.Ala68Thr | |
| ENST00000637494.1:c.199-526G>A | ENSP00000490057.1:n.199-526G>A | |
| ENST00000637667.1:c.218G>A | ENSP00000489843.1:p.Arg73His | |
| ENST00000637823.1:c.224-201G>A | ||
| ENST00000637888.1:c.198+6692G>A | ENSP00000490546.1:n.198+6692G>A | |
| ENST00000638076.1:c.317G>A | ENSP00000490373.1:p.Arg106His | |
| ENST00000638144.1:n.130-526G>A | ||
| ENST00000646164.1:c.38+6692G>A | ||
| ENST00000249806.9:c.317G>A | ENSP00000249806.5:p.Arg106His | |
| ENST00000538696.5:c.413G>A | ENSP00000445770.1:p.Arg138His | |
| ENST00000562767.1:c.84-14216G>A | ENSP00000456336.1:n.84-14216G>A | |
| ENST00000563917.1:n.98G>A | ||
| ENST00000564752.1:c.317G>A | ENSP00000457822.1:p.Arg106His | |
| ENST00000565471.5:c.84-2085G>A | ENSP00000457384.1:n.84-2085G>A | |
| ENST00000566347.5:c.298-526G>A | ENSP00000457783.1:n.298-526G>A | |
| ENST00000567060.5:c.298-2124G>A | ENSP00000454818.1:n.298-2124G>A | |
| NM_017882.2:c.317G>A | NP_060352.1:p.Arg106His | |
| XR_931861.1:n.420G>A | ||
| NM_017882.3:c.317G>A MANE Select | NP_060352.1:p.Arg106His |