Linked Data
ClinVar Variation Id:
382433
dbSNP Id:
rs1057521355
gnomAD v2:
19-1219427-C-T
gnomAD v3:
19-1219428-C-T
gnomAD v4:
19-1219428-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1219428C>T , CM000681.2:g.1219428C>T | GRCh38 |
| NC_000019.9:g.1219427C>T , CM000681.1:g.1219427C>T | GRCh37 |
| NC_000019.8:g.1170427C>T | NCBI36 |
| NG_007460.2:g.35022C>T , LRG_319:g.35022C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000585465.3:c.464+15C>T | ENSP00000490268.2:n.464+15C>T | |
| ENST00000585748.3:c.92+15C>T | ENSP00000477641.2:n.92+15C>T | |
| ENST00000585851.2:c.291-945C>T | ENSP00000467912.2:n.291-945C>T | |
| ENST00000326873.12:c.464+15C>T MANE Select | ENSP00000324856.6:n.464+15C>T | |
| ENST00000652231.1:c.464+15C>T | ENSP00000498804.1:n.464+15C>T | |
| ENST00000326873.11:c.464+15C>T | ENSP00000324856.6:n.464+15C>T | |
| ENST00000585851.1:c.291-945C>T | ENSP00000467912.1:n.291-945C>T | |
| ENST00000586243.5:c.464+15C>T | ENSP00000467240.2:n.464+15C>T | |
| ENST00000586358.5:n.287+15C>T | ||
| ENST00000589152.5:n.554+15C>T | ||
| NM_000455.4:c.464+15C>T , LRG_319t1:c.464+15C>T | NP_000446.1:n.464+15C>T | |
| XM_005259617.1:c.464+15C>T | XP_005259674.1:n.464+15C>T | |
| XM_005259618.3:c.464+15C>T | XP_005259675.1:n.464+15C>T | |
| XM_011528209.1:c.242+15C>T | XP_011526511.1:n.242+15C>T | |
| XR_936204.1:n.1089+15C>T | ||
| XM_005259617.3:c.464+15C>T | XP_005259674.1:n.464+15C>T | |
| XM_011528209.2:c.242+15C>T | XP_011526511.1:n.242+15C>T | |
| XR_001753738.2:n.1089+15C>T | ||
| XR_001753739.1:n.1089+15C>T | ||
| XR_001753740.2:n.1089+15C>T | ||
| NM_000455.5:c.464+15C>T MANE Select | NP_000446.1:n.464+15C>T |