Linked Data
ClinVar Variation Id:
127699
dbSNP Id:
rs587780008
gnomAD v2:
19-1226533-G-T
gnomAD v3:
19-1226534-G-T
gnomAD v4:
19-1226534-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1226534G>T , CM000681.2:g.1226534G>T | GRCh38 |
| NC_000019.9:g.1226533G>T , CM000681.1:g.1226533G>T | GRCh37 |
| NC_000019.8:g.1177533G>T | NCBI36 |
| NG_007460.2:g.42128G>T , LRG_319:g.42128G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000585465.3:c.*2790G>T | ENSP00000490268.2:n.*2790G>T | |
| ENST00000585748.3:c.817G>T | ENSP00000477641.2:p.Ala273Ser | |
| ENST00000585851.2:c.1015G>T | ENSP00000467912.2:p.Ala339Ser | |
| ENST00000326873.12:c.1189G>T MANE Select | ENSP00000324856.6:p.Ala397Ser | |
| ENST00000326873.11:c.1189G>T | ENSP00000324856.6:p.Ala397Ser | |
| ENST00000585465.2:n.2922G>T | ||
| ENST00000586243.5:c.1189G>T | ENSP00000467240.2:p.Ala397Ser | |
| ENST00000589152.5:n.1887G>T | ||
| NM_000455.4:c.1189G>T , LRG_319t1:c.1189G>T | NP_000446.1:p.Ala397Ser | |
| XM_005259617.1:c.1184G>T | XP_005259674.1:p.Gly395Val | |
| XM_011528209.1:c.962G>T | XP_011526511.1:p.Gly321Val | |
| XM_005259617.3:c.1184G>T | XP_005259674.1:p.Gly395Val | |
| XM_011528209.2:c.962G>T | XP_011526511.1:p.Gly321Val | |
| XR_001753738.2:n.1995G>T | ||
| XR_001753740.2:n.1965G>T | ||
| NM_000455.5:c.1189G>T MANE Select | NP_000446.1:p.Ala397Ser |