Linked Data
ClinVar Variation Id:
1935797
ClinVar RCV Id:
RCV002636088
dbSNP Id:
rs2145404738
MyVariant Identifiers:
chr19:g.1206984G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1206985G>T , CM000681.2:g.1206985G>T | GRCh38 |
| NC_000019.9:g.1206984G>T , CM000681.1:g.1206984G>T | GRCh37 |
| NC_000019.8:g.1157984G>T | NCBI36 |
| NG_007460.2:g.22579G>T , LRG_319:g.22579G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000585465.3:c.72G>T | ENSP00000490268.2:p.Thr24= | |
| ENST00000585748.3:c.-82-11432G>T | ENSP00000477641.2:n.-82-11432G>T | |
| ENST00000585851.2:c.72G>T | ENSP00000467912.2:p.Thr24= | |
| ENST00000326873.12:c.72G>T MANE Select | ENSP00000324856.6:p.Thr24= | |
| ENST00000652231.1:c.72G>T | ENSP00000498804.1:p.Thr24= | |
| ENST00000326873.11:c.72G>T | ENSP00000324856.6:p.Thr24= | |
| ENST00000585748.2:c.-82-11432G>T | ENSP00000477641.1:n.-82-11432G>T | |
| ENST00000585851.1:c.72G>T | ENSP00000467912.1:p.Thr24= | |
| ENST00000586243.5:c.72G>T | ENSP00000467240.2:p.Thr24= | |
| ENST00000589152.5:n.162G>T | ||
| ENST00000593219.5:c.72G>T | ENSP00000466610.1:p.Thr24= | |
| NM_000455.4:c.72G>T , LRG_319t1:c.72G>T | NP_000446.1:p.Thr24= | |
| XM_005259617.1:c.72G>T | XP_005259674.1:p.Thr24= | |
| XM_005259618.3:c.72G>T | XP_005259675.1:p.Thr24= | |
| XM_011528209.1:c.-282G>T | XP_011526511.1:n.-282G>T | |
| XR_936204.1:n.697G>T | ||
| XM_005259617.3:c.72G>T | XP_005259674.1:p.Thr24= | |
| XM_011528209.2:c.-282G>T | XP_011526511.1:n.-282G>T | |
| XR_001753738.2:n.697G>T | ||
| XR_001753739.1:n.697G>T | ||
| XR_001753740.2:n.697G>T | ||
| NM_000455.5:c.72G>T MANE Select | NP_000446.1:p.Thr24= |