Linked Data
ClinVar Variation Id:
2985252
ClinVar RCV Id:
RCV003848379
dbSNP Id:
rs967752328
gnomAD v3:
15-68214273-G-A
gnomAD v4:
15-68214273-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.68214273G>A , CM000677.2:g.68214273G>A | GRCh38 |
| NC_000015.9:g.68506611G>A , CM000677.1:g.68506611G>A | GRCh37 |
| NC_000015.8:g.66293665G>A | NCBI36 |
| NG_008764.2:g.47939C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000249806.11:c.297+17C>T MANE Select | ENSP00000249806.5:n.297+17C>T | |
| ENST00000562767.2:c.83+15229C>T | ENSP00000456336.1:n.83+15229C>T | |
| ENST00000563917.2:n.139+17C>T | ||
| ENST00000565471.6:c.84-4514C>T | ENSP00000457384.1:n.84-4514C>T | |
| ENST00000635747.1:c.*200+17C>T | ENSP00000490627.1:n.*200+17C>T | |
| ENST00000635754.1:n.1336C>T | ||
| ENST00000636020.1:n.446C>T | ||
| ENST00000636212.1:c.297+17C>T | ENSP00000489851.1:n.297+17C>T | |
| ENST00000636314.1:c.182+17C>T | ENSP00000490295.1:n.182+17C>T | |
| ENST00000637054.1:c.198+4263C>T | ENSP00000490807.1:n.198+4263C>T | |
| ENST00000637223.1:c.*200+17C>T | ENSP00000490010.1:n.*200+17C>T | |
| ENST00000637329.1:c.208+17C>T | ||
| ENST00000637450.1:c.182+17C>T | ENSP00000490204.1:n.182+17C>T | |
| ENST00000637494.1:c.199-2955C>T | ENSP00000490057.1:n.199-2955C>T | |
| ENST00000637667.1:c.199-2410C>T | ENSP00000489843.1:n.199-2410C>T | |
| ENST00000637823.1:c.223+17C>T | ||
| ENST00000637888.1:c.198+4263C>T | ENSP00000490546.1:n.198+4263C>T | |
| ENST00000638076.1:c.297+17C>T | ENSP00000490373.1:n.297+17C>T | |
| ENST00000638144.1:n.129+17C>T | ||
| ENST00000646164.1:c.38+4263C>T | ||
| ENST00000249806.9:c.297+17C>T | ENSP00000249806.5:n.297+17C>T | |
| ENST00000538696.5:c.393+17C>T | ENSP00000445770.1:n.393+17C>T | |
| ENST00000562767.1:c.83+15229C>T | ENSP00000456336.1:n.83+15229C>T | |
| ENST00000563917.1:n.78+17C>T | ||
| ENST00000564752.1:c.297+17C>T | ENSP00000457822.1:n.297+17C>T | |
| ENST00000564846.1:n.746C>T | ||
| ENST00000565471.5:c.84-4514C>T | ENSP00000457384.1:n.84-4514C>T | |
| ENST00000566347.5:c.297+17C>T | ENSP00000457783.1:n.297+17C>T | |
| ENST00000567060.5:c.297+17C>T | ENSP00000454818.1:n.297+17C>T | |
| NM_017882.2:c.297+17C>T | NP_060352.1:n.297+17C>T | |
| XR_931861.1:n.400+17C>T | ||
| NM_017882.3:c.297+17C>T MANE Select | NP_060352.1:n.297+17C>T |