Linked Data
ClinVar Variation Id:
1343600
ClinVar RCV Id:
RCV001844617
dbSNP Id:
rs2141620363
gnomAD v4:
16-13947879-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.13947879T>G , CM000678.2:g.13947879T>G | GRCh38 |
| NC_000016.9:g.14041736T>G , CM000678.1:g.14041736T>G | GRCh37 |
| NC_000016.8:g.13949237T>G | NCBI36 |
| NG_011442.1:g.32723T>G , LRG_463:g.32723T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682617.1:c.2421T>G | ENSP00000507912.1:p.Phe807Leu | |
| ENST00000683962.1:c.*1977T>G | ENSP00000506854.1:n.*1977T>G | |
| ENST00000311895.8:c.2283T>G MANE Select | ENSP00000310520.7:p.Phe761Leu | |
| ENST00000311895.7:c.2283T>G | ENSP00000310520.7:p.Phe761Leu | |
| ENST00000389138.7:n.1560T>G | ||
| ENST00000462862.1:c.596T>G | ENSP00000461322.1:n.596T>G | |
| NM_005236.2:c.2283T>G , LRG_463t1:c.2283T>G | NP_005227.1:p.Phe761Leu | |
| XM_011522424.1:c.2421T>G | XP_011520726.1:p.Phe807Leu | |
| XM_011522425.1:c.1740T>G | XP_011520727.1:p.Phe580Leu | |
| XM_011522426.1:c.1494T>G | XP_011520728.1:p.Phe498Leu | |
| XM_011522427.1:c.933T>G | XP_011520729.1:p.Phe311Leu | |
| XR_932805.1:n.2442T>G | ||
| XM_011522424.3:c.2421T>G | XP_011520726.1:p.Phe807Leu | |
| XM_017023043.2:c.1494T>G | XP_016878532.1:p.Phe498Leu | |
| NM_005236.3:c.2283T>G MANE Select | NP_005227.1:p.Phe761Leu |