Linked Data
ClinVar Variation Id:
127701
dbSNP Id:
rs372329880
ExAC:
19:1226573 C / T
gnomAD v2:
19-1226573-C-T
gnomAD v3:
19-1226574-C-T
gnomAD v4:
19-1226574-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1226574C>T , CM000681.2:g.1226574C>T | GRCh38 |
| NC_000019.9:g.1226573C>T , CM000681.1:g.1226573C>T | GRCh37 |
| NC_000019.8:g.1177573C>T | NCBI36 |
| NG_007460.2:g.42168C>T , LRG_319:g.42168C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000585465.3:c.*2830C>T | ENSP00000490268.2:n.*2830C>T | |
| ENST00000585748.3:c.857C>T | ENSP00000477641.2:p.Ala286Val | |
| ENST00000585851.2:c.1055C>T | ENSP00000467912.2:p.Ala352Val | |
| ENST00000326873.12:c.1229C>T MANE Select | ENSP00000324856.6:p.Ala410Val | |
| ENST00000326873.11:c.1229C>T | ENSP00000324856.6:p.Ala410Val | |
| ENST00000585465.2:n.2962C>T | ||
| ENST00000586243.5:c.1228C>T | ENSP00000467240.2:p.Pro410Ser | |
| ENST00000589152.5:n.1927C>T | ||
| NM_000455.4:c.1229C>T , LRG_319t1:c.1229C>T | NP_000446.1:p.Ala410Val | |
| XM_005259617.1:c.1224C>T | XP_005259674.1:p.Gly408= | |
| XM_011528209.1:c.1002C>T | XP_011526511.1:p.Gly334= | |
| XM_005259617.3:c.1224C>T | XP_005259674.1:p.Gly408= | |
| XM_011528209.2:c.1002C>T | XP_011526511.1:p.Gly334= | |
| XR_001753738.2:n.2035C>T | ||
| XR_001753740.2:n.2005C>T | ||
| NM_000455.5:c.1229C>T MANE Select | NP_000446.1:p.Ala410Val |