Linked Data
ClinVar Variation Id:
94166
dbSNP Id:
rs398123717
ExAC:
12:49424760 G / T
gnomAD v2:
12-49424760-G-T
gnomAD v3:
12-49030977-G-T
gnomAD v4:
12-49030977-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.49030977G>T , CM000674.2:g.49030977G>T | GRCh38 |
| NC_000012.11:g.49424760G>T , CM000674.1:g.49424760G>T | GRCh37 |
| NC_000012.10:g.47711027G>T | NCBI36 |
| NG_027827.1:g.29348C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000552391.2:n.287C>A | ||
| ENST00000683543.2:c.13587C>A | ENSP00000506726.1:p.Ser4529Arg | |
| ENST00000685166.1:c.13596C>A | ENSP00000509386.1:p.Ser4532Arg | |
| ENST00000685982.1:c.138+198C>A | ENSP00000508613.1:n.138+198C>A | |
| ENST00000691986.1:c.138+198C>A | ENSP00000509196.1:n.138+198C>A | |
| ENST00000692637.1:c.13584C>A | ENSP00000509666.1:p.Ser4528Arg | |
| ENST00000692973.1:c.188C>A | ENSP00000508893.1:n.188C>A | |
| ENST00000301067.12:c.13587C>A MANE Select | ENSP00000301067.7:p.Ser4529Arg | |
| ENST00000301067.11:c.13587C>A | ENSP00000301067.7:p.Ser4529Arg | |
| ENST00000552391.1:n.287C>A | ||
| NM_003482.3:c.13587C>A | NP_003473.3:p.Ser4529Arg | |
| XM_005269162.3:c.13587C>A | XP_005269219.1:p.Ser4529Arg | |
| XM_006719614.2:c.13596C>A | XP_006719677.1:p.Ser4532Arg | |
| XM_006719616.2:c.13584C>A | XP_006719679.1:p.Ser4528Arg | |
| XM_011538770.1:c.13596C>A | XP_011537072.1:p.Ser4532Arg | |
| XM_011538771.1:c.13593C>A | XP_011537073.1:p.Ser4531Arg | |
| XM_011538772.1:c.13587C>A | XP_011537074.1:p.Ser4529Arg | |
| XM_011538773.1:c.13584C>A | XP_011537075.1:p.Ser4528Arg | |
| XM_011538774.1:c.13575C>A | XP_011537076.1:p.Ser4525Arg | |
| XM_011538775.1:c.13596C>A | XP_011537077.1:p.Ser4532Arg | |
| XM_011538776.1:c.13503C>A | XP_011537078.1:p.Ser4501Arg | |
| XR_944740.1:n.15916C>A | ||
| XM_005269162.4:c.13587C>A | XP_005269219.1:p.Ser4529Arg | |
| XM_006719614.4:c.13596C>A | XP_006719677.1:p.Ser4532Arg | |
| XM_006719616.3:c.13584C>A | XP_006719679.1:p.Ser4528Arg | |
| XM_011538770.2:c.13596C>A | XP_011537072.1:p.Ser4532Arg | |
| XM_011538771.2:c.13593C>A | XP_011537073.1:p.Ser4531Arg | |
| XM_011538772.2:c.13587C>A | XP_011537074.1:p.Ser4529Arg | |
| XM_011538773.2:c.13584C>A | XP_011537075.1:p.Ser4528Arg | |
| XM_011538774.2:c.13575C>A | XP_011537076.1:p.Ser4525Arg | |
| XM_011538776.2:c.13503C>A | XP_011537078.1:p.Ser4501Arg | |
| XR_001748874.1:n.14905C>A | ||
| NM_003482.4:c.13587C>A MANE Select | NP_003473.3:p.Ser4529Arg |