Linked Data
ClinVar Variation Id:
1126796
ClinVar RCV Id:
RCV001458956
dbSNP Id:
rs774441548
ExAC:
1:216420078 C / T
gnomAD v2:
1-216420078-C-T
gnomAD v4:
1-216246736-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.216246736C>T , CM000663.2:g.216246736C>T | GRCh38 |
| NC_000001.10:g.216420078C>T , CM000663.1:g.216420078C>T | GRCh37 |
| NC_000001.9:g.214486701C>T | NCBI36 |
| NG_009497.1:g.181661G>A | |
| NG_009497.2:g.181713G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.2658G>A MANE Select | ENSP00000305941.3:p.Arg886= | |
| ENST00000674083.1:c.2658G>A | ENSP00000501296.1:p.Arg886= | |
| ENST00000307340.7:c.2658G>A | ENSP00000305941.3:p.Arg886= | |
| ENST00000366942.3:c.2658G>A | ENSP00000355909.3:p.Arg886= | |
| NM_007123.5:c.2658G>A | NP_009054.5:p.Arg886= | |
| NM_206933.2:c.2658G>A | NP_996816.2:p.Arg886= | |
| NM_206933.3:c.2658G>A | NP_996816.2:p.Arg886= | |
| NM_007123.6:c.2658G>A | NP_009054.6:p.Arg886= | |
| NM_206933.4:c.2658G>A MANE Select | NP_996816.3:p.Arg886= |