Linked Data
ClinVar Variation Id:
3231739
ClinVar RCV Id:
RCV004518454
dbSNP Id:
rs1371667554
gnomAD v4:
19-1226630-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1226630G>T , CM000681.2:g.1226630G>T | GRCh38 |
| NC_000019.9:g.1226629G>T , CM000681.1:g.1226629G>T | GRCh37 |
| NC_000019.8:g.1177629G>T | NCBI36 |
| NG_007460.2:g.42224G>T , LRG_319:g.42224G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000585465.3:c.*2886G>T | ENSP00000490268.2:n.*2886G>T | |
| ENST00000585748.3:c.913G>T | ENSP00000477641.2:p.Ala305Ser | |
| ENST00000585851.2:c.1111G>T | ENSP00000467912.2:p.Ala371Ser | |
| ENST00000326873.12:c.1285G>T MANE Select | ENSP00000324856.6:p.Ala429Ser | |
| ENST00000326873.11:c.1285G>T | ENSP00000324856.6:p.Ala429Ser | |
| ENST00000585465.2:n.3018G>T | ||
| ENST00000586243.5:c.1282G>T | ENSP00000467240.2:p.Ala428Ser | |
| ENST00000589152.5:n.1983G>T | ||
| NM_000455.4:c.1285G>T , LRG_319t1:c.1285G>T | NP_000446.1:p.Ala429Ser | |
| XM_005259617.1:c.1280G>T | XP_005259674.1:p.Gly427Val | |
| XM_011528209.1:c.1058G>T | XP_011526511.1:p.Gly353Val | |
| XM_005259617.3:c.1280G>T | XP_005259674.1:p.Gly427Val | |
| XM_011528209.2:c.1058G>T | XP_011526511.1:p.Gly353Val | |
| XR_001753738.2:n.2091G>T | ||
| XR_001753740.2:n.2061G>T | ||
| NM_000455.5:c.1285G>T MANE Select | NP_000446.1:p.Ala429Ser |