Linked Data
ClinVar Variation Id:
196686
dbSNP Id:
rs794727547
gnomAD v2:
12-49434814-G-A
gnomAD v3:
12-49041031-G-A
gnomAD v4:
12-49041031-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.49041031G>A , CM000674.2:g.49041031G>A | GRCh38 |
| NC_000012.11:g.49434814G>A , CM000674.1:g.49434814G>A | GRCh37 |
| NC_000012.10:g.47721081G>A | NCBI36 |
| NG_027827.1:g.19294C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000683543.2:c.6739C>T | ENSP00000506726.1:p.Pro2247Ser | |
| ENST00000685166.1:c.6748C>T | ENSP00000509386.1:p.Pro2250Ser | |
| ENST00000689060.1:c.758C>T | ||
| ENST00000689143.1:c.412C>T | ENSP00000509839.1:p.Pro138Ser | |
| ENST00000689944.1:c.848C>T | ||
| ENST00000692637.1:c.6736C>T | ENSP00000509666.1:p.Pro2246Ser | |
| ENST00000301067.12:c.6739C>T MANE Select | ENSP00000301067.7:p.Pro2247Ser | |
| ENST00000301067.11:c.6739C>T | ENSP00000301067.7:p.Pro2247Ser | |
| NM_003482.3:c.6739C>T | NP_003473.3:p.Pro2247Ser | |
| XM_005269162.3:c.6739C>T | XP_005269219.1:p.Pro2247Ser | |
| XM_006719614.2:c.6748C>T | XP_006719677.1:p.Pro2250Ser | |
| XM_006719616.2:c.6736C>T | XP_006719679.1:p.Pro2246Ser | |
| XM_011538770.1:c.6748C>T | XP_011537072.1:p.Pro2250Ser | |
| XM_011538771.1:c.6745C>T | XP_011537073.1:p.Pro2249Ser | |
| XM_011538772.1:c.6739C>T | XP_011537074.1:p.Pro2247Ser | |
| XM_011538773.1:c.6736C>T | XP_011537075.1:p.Pro2246Ser | |
| XM_011538774.1:c.6727C>T | XP_011537076.1:p.Pro2243Ser | |
| XM_011538775.1:c.6748C>T | XP_011537077.1:p.Pro2250Ser | |
| XM_011538776.1:c.6655C>T | XP_011537078.1:p.Pro2219Ser | |
| XR_944740.1:n.9068C>T | ||
| XM_005269162.4:c.6739C>T | XP_005269219.1:p.Pro2247Ser | |
| XM_006719614.4:c.6748C>T | XP_006719677.1:p.Pro2250Ser | |
| XM_006719616.3:c.6736C>T | XP_006719679.1:p.Pro2246Ser | |
| XM_011538770.2:c.6748C>T | XP_011537072.1:p.Pro2250Ser | |
| XM_011538771.2:c.6745C>T | XP_011537073.1:p.Pro2249Ser | |
| XM_011538772.2:c.6739C>T | XP_011537074.1:p.Pro2247Ser | |
| XM_011538773.2:c.6736C>T | XP_011537075.1:p.Pro2246Ser | |
| XM_011538774.2:c.6727C>T | XP_011537076.1:p.Pro2243Ser | |
| XM_011538776.2:c.6655C>T | XP_011537078.1:p.Pro2219Ser | |
| XR_001748874.1:n.8057C>T | ||
| NM_003482.4:c.6739C>T MANE Select | NP_003473.3:p.Pro2247Ser |