Linked Data
ClinVar Variation Id:
485004
dbSNP Id:
rs754853898
ExAC:
19:1226617 C / A
gnomAD v2:
19-1226617-C-A
gnomAD v4:
19-1226618-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1226618C>A , CM000681.2:g.1226618C>A | GRCh38 |
| NC_000019.9:g.1226617C>A , CM000681.1:g.1226617C>A | GRCh37 |
| NC_000019.8:g.1177617C>A | NCBI36 |
| NG_007460.2:g.42212C>A , LRG_319:g.42212C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000585465.3:c.*2874C>A | ENSP00000490268.2:n.*2874C>A | |
| ENST00000585748.3:c.901C>A | ENSP00000477641.2:p.Arg301Ser | |
| ENST00000585851.2:c.1099C>A | ENSP00000467912.2:p.Arg367Ser | |
| ENST00000326873.12:c.1273C>A MANE Select | ENSP00000324856.6:p.Arg425Ser | |
| ENST00000326873.11:c.1273C>A | ENSP00000324856.6:p.Arg425Ser | |
| ENST00000585465.2:n.3006C>A | ||
| ENST00000586243.5:c.1270C>A | ENSP00000467240.2:p.Arg424Ser | |
| ENST00000589152.5:n.1971C>A | ||
| NM_000455.4:c.1273C>A , LRG_319t1:c.1273C>A | NP_000446.1:p.Arg425Ser | |
| XM_005259617.1:c.1268C>A | XP_005259674.1:p.Pro423Gln | |
| XM_011528209.1:c.1046C>A | XP_011526511.1:p.Pro349Gln | |
| XM_005259617.3:c.1268C>A | XP_005259674.1:p.Pro423Gln | |
| XM_011528209.2:c.1046C>A | XP_011526511.1:p.Pro349Gln | |
| XR_001753738.2:n.2079C>A | ||
| XR_001753740.2:n.2049C>A | ||
| NM_000455.5:c.1273C>A MANE Select | NP_000446.1:p.Arg425Ser |