Linked Data
ClinVar Variation Id:
1454452
ClinVar RCV Id:
RCV001960667
dbSNP Id:
rs772898391
ExAC:
17:7125303 C / A
gnomAD v2:
17-7125303-C-A
gnomAD v3:
17-7221984-C-A
gnomAD v4:
17-7221984-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7221984C>A , CM000679.2:g.7221984C>A | GRCh38 |
| NC_000017.10:g.7125303C>A , CM000679.1:g.7125303C>A | GRCh37 |
| NC_000017.9:g.7066027C>A | NCBI36 |
| NG_007975.1:g.7151C>A | |
| NG_008391.2:g.3067G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000356839.10:c.655C>A MANE Select | ENSP00000349297.5:p.Pro219Thr | |
| ENST00000322910.9:c.*610C>A | ENSP00000325395.5:n.*610C>A | |
| ENST00000350303.9:c.589C>A | ENSP00000344152.5:p.Pro197Thr | |
| ENST00000356839.9:c.655C>A | ENSP00000349297.5:p.Pro219Thr | |
| ENST00000543245.6:c.724C>A | ENSP00000438689.2:p.Pro242Thr | |
| ENST00000577191.5:n.732C>A | ||
| ENST00000577857.5:n.471C>A | ||
| ENST00000579286.5:n.836C>A | ||
| ENST00000580365.1:n.386C>A | ||
| ENST00000581378.5:c.373C>A | ||
| ENST00000581562.5:n.557C>A | ||
| ENST00000582379.1:n.39C>A | ||
| ENST00000583312.5:c.670C>A | ENSP00000467920.1:p.Pro224Thr | |
| ENST00000583760.1:n.437C>A | ||
| NM_000018.3:c.655C>A | NP_000009.1:p.Pro219Thr | |
| NM_001033859.2:c.589C>A | NP_001029031.1:p.Pro197Thr | |
| NM_001270447.1:c.724C>A | NP_001257376.1:p.Pro242Thr | |
| NM_001270448.1:c.427C>A | NP_001257377.1:p.Pro143Thr | |
| XM_006721516.2:c.655C>A | XP_006721579.2:p.Pro219Thr | |
| XM_011523829.1:c.655C>A | XP_011522131.1:p.Pro219Thr | |
| XM_011523830.1:c.655C>A | XP_011522132.1:p.Pro219Thr | |
| XR_934021.1:n.762C>A | ||
| XR_934022.1:n.762C>A | ||
| XR_934023.1:n.762C>A | ||
| XM_006721516.3:c.655C>A | XP_006721579.2:p.Pro219Thr | |
| XM_011523829.2:c.655C>A | XP_011522131.1:p.Pro219Thr | |
| XM_011523830.2:c.655C>A | XP_011522132.1:p.Pro219Thr | |
| XM_024450741.1:c.655C>A | XP_024306509.1:p.Pro219Thr | |
| XR_934021.2:n.714C>A | ||
| XR_934022.2:n.714C>A | ||
| XR_934023.2:n.714C>A | ||
| NM_000018.4:c.655C>A MANE Select | NP_000009.1:p.Pro219Thr | |
| NM_001033859.3:c.589C>A | NP_001029031.1:p.Pro197Thr | |
| NM_001270447.2:c.724C>A | NP_001257376.1:p.Pro242Thr | |
| NM_001270448.2:c.427C>A | NP_001257377.1:p.Pro143Thr |