Linked Data
ClinVar Variation Id:
205164
ClinVar RCV Id:
RCV000187092
dbSNP Id:
rs796052351
gnomAD v4:
15-68214289-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.68214289C>T , CM000677.2:g.68214289C>T | GRCh38 |
| NC_000015.9:g.68506627C>T , CM000677.1:g.68506627C>T | GRCh37 |
| NC_000015.8:g.66293681C>T | NCBI36 |
| NG_008764.2:g.47923G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000249806.11:c.297+1G>A MANE Select | ENSP00000249806.5:n.297+1G>A | |
| ENST00000562767.2:c.83+15213G>A | ENSP00000456336.1:n.83+15213G>A | |
| ENST00000563917.2:n.139+1G>A | ||
| ENST00000565471.6:c.84-4530G>A | ENSP00000457384.1:n.84-4530G>A | |
| ENST00000635747.1:c.*200+1G>A | ENSP00000490627.1:n.*200+1G>A | |
| ENST00000635754.1:n.1320G>A | ||
| ENST00000636020.1:n.430G>A | ||
| ENST00000636212.1:c.297+1G>A | ENSP00000489851.1:n.297+1G>A | |
| ENST00000636314.1:c.182+1G>A | ENSP00000490295.1:n.182+1G>A | |
| ENST00000637054.1:c.198+4247G>A | ENSP00000490807.1:n.198+4247G>A | |
| ENST00000637223.1:c.*200+1G>A | ENSP00000490010.1:n.*200+1G>A | |
| ENST00000637329.1:c.208+1G>A | ||
| ENST00000637450.1:c.182+1G>A | ENSP00000490204.1:n.182+1G>A | |
| ENST00000637494.1:c.199-2971G>A | ENSP00000490057.1:n.199-2971G>A | |
| ENST00000637667.1:c.199-2426G>A | ENSP00000489843.1:n.199-2426G>A | |
| ENST00000637823.1:c.223+1G>A | ||
| ENST00000637888.1:c.198+4247G>A | ENSP00000490546.1:n.198+4247G>A | |
| ENST00000638076.1:c.297+1G>A | ENSP00000490373.1:n.297+1G>A | |
| ENST00000638144.1:n.129+1G>A | ||
| ENST00000646164.1:c.38+4247G>A | ||
| ENST00000249806.9:c.297+1G>A | ENSP00000249806.5:n.297+1G>A | |
| ENST00000538696.5:c.393+1G>A | ENSP00000445770.1:n.393+1G>A | |
| ENST00000562767.1:c.83+15213G>A | ENSP00000456336.1:n.83+15213G>A | |
| ENST00000563917.1:n.78+1G>A | ||
| ENST00000564752.1:c.297+1G>A | ENSP00000457822.1:n.297+1G>A | |
| ENST00000564846.1:n.730G>A | ||
| ENST00000565471.5:c.84-4530G>A | ENSP00000457384.1:n.84-4530G>A | |
| ENST00000566347.5:c.297+1G>A | ENSP00000457783.1:n.297+1G>A | |
| ENST00000567060.5:c.297+1G>A | ENSP00000454818.1:n.297+1G>A | |
| NM_017882.2:c.297+1G>A | NP_060352.1:n.297+1G>A | |
| XR_931861.1:n.400+1G>A | ||
| NM_017882.3:c.297+1G>A MANE Select | NP_060352.1:n.297+1G>A |