Linked Data
ClinVar Variation Id:
2850918
ClinVar RCV Id:
RCV003646588
dbSNP Id:
rs997398671
gnomAD v3:
17-8237413-A-C
gnomAD v4:
17-8237413-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8237413A>C , CM000679.2:g.8237413A>C | GRCh38 |
| NC_000017.10:g.8140731A>C , CM000679.1:g.8140731A>C | GRCh37 |
| NC_000017.9:g.8081456A>C | NCBI36 |
| NG_032148.1:g.15683T>G | |
| NG_032148.2:g.15683T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000580299.2:c.754T>G | ENSP00000462607.2:p.Ser252Ala | |
| ENST00000581729.2:c.754T>G | ENSP00000462720.2:p.Ser252Ala | |
| ENST00000581967.2:n.776T>G | ||
| ENST00000583254.2:n.168T>G | ||
| ENST00000699849.1:c.-144T>G | ENSP00000514647.1:n.-144T>G | |
| ENST00000699850.1:n.56-1071T>G | ||
| ENST00000699851.1:n.776T>G | ||
| ENST00000699852.1:c.754T>G | ENSP00000514648.1:p.Ser252Ala | |
| ENST00000699853.1:c.754T>G | ENSP00000514649.1:p.Ser252Ala | |
| ENST00000699854.1:n.547T>G | ||
| ENST00000699855.1:n.776T>G | ||
| ENST00000699856.1:c.754T>G | ENSP00000514650.1:p.Ser252Ala | |
| ENST00000699857.1:n.762T>G | ||
| ENST00000699858.1:c.754T>G | ENSP00000514651.1:p.Ser252Ala | |
| ENST00000699859.1:c.754T>G | ENSP00000514652.1:p.Ser252Ala | |
| ENST00000699861.1:n.776T>G | ||
| ENST00000699862.1:n.641T>G | ||
| ENST00000449476.7:c.649T>G | ENSP00000396018.2:p.Ser217Ala | |
| ENST00000581671.2:n.595T>G | ||
| ENST00000643543.1:c.754T>G | ENSP00000494323.1:p.Ser252Ala | |
| ENST00000651323.1:c.754T>G MANE Select | ENSP00000498499.1:p.Ser252Ala | |
| ENST00000315684.12:c.754T>G | ENSP00000313759.8:p.Ser252Ala | |
| ENST00000449476.6:c.649T>G | ENSP00000396018.2:p.Ser217Ala | |
| ENST00000581671.1:n.595T>G | ||
| NM_025099.5:c.754T>G | NP_079375.3:p.Ser252Ala | |
| NR_046431.1:n.708T>G | ||
| XM_006721577.2:c.754T>G | XP_006721640.1:p.Ser252Ala | |
| XM_006721578.2:c.754T>G | XP_006721641.1:p.Ser252Ala | |
| XM_006721579.2:c.754T>G | XP_006721642.1:p.Ser252Ala | |
| XM_011524010.1:c.649T>G | XP_011522312.1:p.Ser217Ala | |
| XM_011524011.1:c.-148T>G | XP_011522313.1:n.-148T>G | |
| XR_429823.2:n.797T>G | ||
| XR_429824.2:n.797T>G | ||
| XR_429825.1:n.797T>G | ||
| NM_025099.6:c.754T>G MANE Select | NP_079375.3:p.Ser252Ala | |
| XM_006721577.3:c.754T>G | XP_006721640.1:p.Ser252Ala | |
| XM_006721578.3:c.754T>G | XP_006721641.1:p.Ser252Ala | |
| XM_011524010.2:c.649T>G | XP_011522312.1:p.Ser217Ala | |
| XM_011524011.2:c.-148T>G | XP_011522313.1:n.-148T>G | |
| XR_001752639.1:n.797T>G | ||
| XR_001752640.1:n.797T>G | ||
| XR_001752641.1:n.797T>G | ||
| XR_001752642.1:n.797T>G | ||
| XR_001752643.1:n.797T>G | ||
| XR_001752644.1:n.797T>G | ||
| XR_002958073.1:n.797T>G | ||
| XR_429823.3:n.797T>G | ||
| XR_429824.3:n.797T>G | ||
| NR_046431.2:n.669T>G |