Linked Data
ClinVar Variation Id:
433289
dbSNP Id:
rs72664286
ExAC:
16:16263678 A / C
gnomAD v2:
16-16263678-A-C
gnomAD v3:
16-16169821-A-C
gnomAD v4:
16-16169821-A-C
PubMed:
PMID:16086317
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.16169821A>C , CM000678.2:g.16169821A>C | GRCh38 |
| NC_000016.9:g.16263678A>C , CM000678.1:g.16263678A>C | GRCh37 |
| NC_000016.8:g.16171179A>C | NCBI36 |
| NG_007558.2:g.58651T>G | |
| NG_007558.3:g.58797T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000622290.5:c.2820T>G | ENSP00000483331.2:p.Arg940= | |
| ENST00000205557.12:c.2820T>G MANE Select | ENSP00000205557.7:p.Arg940= | |
| ENST00000205557.11:c.2820T>G | ENSP00000205557.7:p.Arg940= | |
| ENST00000456970.6:c.2645T>G | ENSP00000405002.2:n.2645T>G | |
| ENST00000622290.4:c.*29T>G | ENSP00000483331.1:n.*29T>G | |
| NM_001171.5:c.2820T>G | NP_001162.4:p.Arg940= | |
| XM_011522479.1:c.2787T>G | XP_011520781.1:p.Arg929= | |
| XM_011522480.1:c.2478T>G | XP_011520782.1:p.Arg826= | |
| XM_011522481.1:c.2478T>G | XP_011520783.1:p.Arg826= | |
| XR_932836.1:n.3055T>G | ||
| XR_932837.1:n.3056T>G | ||
| XR_932838.1:n.3056T>G | ||
| NM_001351800.1:c.2478T>G | NP_001338729.1:p.Arg826= | |
| NR_147784.1:n.2682T>G | ||
| XM_011522479.2:c.2787T>G | XP_011520781.1:p.Arg929= | |
| XM_011522481.3:c.2478T>G | XP_011520783.1:p.Arg826= | |
| XM_017023212.1:c.2652T>G | XP_016878701.1:p.Arg884= | |
| XM_017023214.1:c.2820T>G | XP_016878703.1:p.Arg940= | |
| XM_024450261.1:c.2856T>G | XP_024306029.1:p.Arg952= | |
| XR_932836.2:n.3001T>G | ||
| XR_932837.3:n.3001T>G | ||
| XR_932838.3:n.3001T>G | ||
| NM_001171.6:c.2820T>G MANE Select | NP_001162.5:p.Arg940= |