Linked Data
ClinVar Variation Id:
136798
dbSNP Id:
rs200775021
ExAC:
15:68503671 G / A
gnomAD v2:
15-68503671-G-A
gnomAD v3:
15-68211333-G-A
gnomAD v4:
15-68211333-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.68211333G>A , CM000677.2:g.68211333G>A | GRCh38 |
| NC_000015.9:g.68503671G>A , CM000677.1:g.68503671G>A | GRCh37 |
| NC_000015.8:g.66290725G>A | NCBI36 |
| NG_008764.2:g.50879C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000249806.11:c.487-15C>T MANE Select | ENSP00000249806.5:n.487-15C>T | |
| ENST00000562767.2:c.84-13705C>T | ENSP00000456336.1:n.84-13705C>T | |
| ENST00000563917.2:n.329-15C>T | ||
| ENST00000565471.6:c.84-1574C>T | ENSP00000457384.1:n.84-1574C>T | |
| ENST00000635747.1:c.*390-15C>T | ENSP00000490627.1:n.*390-15C>T | |
| ENST00000636212.1:c.*157-15C>T | ENSP00000489851.1:n.*157-15C>T | |
| ENST00000636314.1:c.183-15C>T | ENSP00000490295.1:n.183-15C>T | |
| ENST00000636674.1:n.1589-15C>T | ||
| ENST00000636964.1:n.2000C>T | ||
| ENST00000637054.1:c.198+7203C>T | ENSP00000490807.1:n.198+7203C>T | |
| ENST00000637223.1:c.*201-15C>T | ENSP00000490010.1:n.*201-15C>T | |
| ENST00000637329.1:c.456-15C>T | ||
| ENST00000637450.1:c.*141-15C>T | ENSP00000490204.1:n.*141-15C>T | |
| ENST00000637494.1:c.199-15C>T | ENSP00000490057.1:n.199-15C>T | |
| ENST00000637667.1:c.388-15C>T | ENSP00000489843.1:n.388-15C>T | |
| ENST00000637823.1:c.312-15C>T | ||
| ENST00000637888.1:c.198+7203C>T | ENSP00000490546.1:n.198+7203C>T | |
| ENST00000638076.1:c.*90-15C>T | ENSP00000490373.1:n.*90-15C>T | |
| ENST00000638144.1:n.130-15C>T | ||
| ENST00000646164.1:c.38+7203C>T | ||
| ENST00000249806.9:c.487-15C>T | ENSP00000249806.5:n.487-15C>T | |
| ENST00000538696.5:c.583-15C>T | ENSP00000445770.1:n.583-15C>T | |
| ENST00000562767.1:c.84-13705C>T | ENSP00000456336.1:n.84-13705C>T | |
| ENST00000563917.1:n.387-15C>T | ||
| ENST00000564752.1:c.513-15C>T | ENSP00000457822.1:n.513-15C>T | |
| ENST00000565471.5:c.84-1574C>T | ENSP00000457384.1:n.84-1574C>T | |
| ENST00000566347.5:c.298-15C>T | ENSP00000457783.1:n.298-15C>T | |
| ENST00000567060.5:c.298-1613C>T | ENSP00000454818.1:n.298-1613C>T | |
| NM_017882.2:c.487-15C>T | NP_060352.1:n.487-15C>T | |
| XR_931861.1:n.709-15C>T | ||
| NM_017882.3:c.487-15C>T MANE Select | NP_060352.1:n.487-15C>T |