Linked Data
ClinVar Variation Id:
1753684
ClinVar RCV Id:
RCV002361927
dbSNP Id:
rs2145436295
gnomAD v4:
19-1226568-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1226568G>A , CM000681.2:g.1226568G>A | GRCh38 |
| NC_000019.9:g.1226567G>A , CM000681.1:g.1226567G>A | GRCh37 |
| NC_000019.8:g.1177567G>A | NCBI36 |
| NG_007460.2:g.42162G>A , LRG_319:g.42162G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000585465.3:c.*2824G>A | ENSP00000490268.2:n.*2824G>A | |
| ENST00000585748.3:c.851G>A | ENSP00000477641.2:p.Gly284Asp | |
| ENST00000585851.2:c.1049G>A | ENSP00000467912.2:p.Gly350Asp | |
| ENST00000326873.12:c.1223G>A MANE Select | ENSP00000324856.6:p.Gly408Asp | |
| ENST00000326873.11:c.1223G>A | ENSP00000324856.6:p.Gly408Asp | |
| ENST00000585465.2:n.2956G>A | ||
| ENST00000586243.5:c.1222G>A | ENSP00000467240.2:p.Ala408Thr | |
| ENST00000589152.5:n.1921G>A | ||
| NM_000455.4:c.1223G>A , LRG_319t1:c.1223G>A | NP_000446.1:p.Gly408Asp | |
| XM_005259617.1:c.1218G>A | XP_005259674.1:p.Gly406= | |
| XM_011528209.1:c.996G>A | XP_011526511.1:p.Gly332= | |
| XM_005259617.3:c.1218G>A | XP_005259674.1:p.Gly406= | |
| XM_011528209.2:c.996G>A | XP_011526511.1:p.Gly332= | |
| XR_001753738.2:n.2029G>A | ||
| XR_001753740.2:n.1999G>A | ||
| NM_000455.5:c.1223G>A MANE Select | NP_000446.1:p.Gly408Asp |