Linked Data
ClinVar Variation Id:
1373484
ClinVar RCV Id:
RCV001880766
dbSNP Id:
rs779163443
ExAC:
7:83036472 C / A
gnomAD v2:
7-83036472-C-A
gnomAD v3:
7-83407156-C-A
gnomAD v4:
7-83407156-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.83407156C>A , CM000669.2:g.83407156C>A | GRCh38 |
| NC_000007.13:g.83036472C>A , CM000669.1:g.83036472C>A | GRCh37 |
| NC_000007.12:g.82874408C>A | NCBI36 |
| NG_021242.1:g.247008G>T | |
| NG_021242.2:g.247008G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000427262.6:c.574G>T | ENSP00000405052.1:p.Ala192Ser | |
| ENST00000642232.1:c.754G>T | ENSP00000494064.1:p.Ala252Ser | |
| ENST00000643230.2:c.754G>T MANE Select | ENSP00000496491.1:p.Ala252Ser | |
| ENST00000643441.1:n.739G>T | ||
| ENST00000644381.1:n.317G>T | ||
| ENST00000307792.7:c.754G>T | ENSP00000303212.3:p.Ala252Ser | |
| ENST00000427262.5:c.574G>T | ENSP00000405052.1:p.Ala192Ser | |
| NM_001178129.1:c.574G>T | NP_001171600.1:p.Ala192Ser | |
| NM_012431.2:c.754G>T | NP_036563.1:p.Ala252Ser | |
| XM_011516715.1:c.754G>T | XP_011515017.1:p.Ala252Ser | |
| NM_012431.3:c.754G>T MANE Select | NP_036563.1:p.Ala252Ser | |
| NM_001178129.2:c.574G>T | NP_001171600.1:p.Ala192Ser |